Mefedrooni (4-MMC) süntees haloketoonist etüülatsetaadis. 1-10 kg skaala.

WillD

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Reaction scheme:
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Reagents:
1. 4'-Methylpropiophenone (cas 5337-93-9) 1 kg;
2. Hydrobromic acid 48% 1300 ml;
3. Hydrogen peroxide 35% 750 ml;
4. Sodium/potassium hydroxide 25% (NaOH/KOH) aqueous solution;
5. Distilled water;
6. Ethyl acetate 6 l;
7. Methylamine 40% aq - 2 l;
8. Acetone - 8 l;
9. Hydrochloric acid (HCl 38%) 500 ml;
10. Isopropyl alcohol;


Equipment and glassware:
1. Scales;
2. Jacketed 10 L reactor equipped with reflux condenser, drip funnel, thermometer, top stirrer and temperature control system;
3. Heating pump;
3. Chiller pump;
4. Vacuum source;
5. Buckets;
6. Freezer;
7. Pyrex dishes;
8. Nutsche filter;
9. pH indicator papers;


Stage 1. Halogenation
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1. 4'-Methylpropiophenone 1000 g is added into a 10 L reactor flask.
2. Hydrobromic (HBr) acid 1300 g 48% is poured into the flask and stirred for 5 min.
3. Hydrogen peroxide 750 g 35% is added into a drip funnel 1 l.
4. Hydrogen peroxide is added dropwise to the stirred reaction mixture.
5. Bromine is released during hydrogen peroxide addition to the mixture, dissolved in solution and reacted.
6. Hydrogen peroxide must be added at an appropriate rate so that the reaction mixture becomes colorless.
7. Reaction mixture temperature have to be kept less than 65 °C. An external cooling is applied in case of overheating. If reaction temperature is higher, hydrogen peroxide addition is stopped.
8. The second part of discoloration reaction can be conducted for longer time. Hydrogen peroxide is added according with reaction temperature.
9. Reaction mixture is left for a 12 h with a constant stirring at room temperature as soon as all hydrogen peroxide is added.
10. After 12 h precipitate is formed.
11. Sodium bicarbonate aq solution is added to the reaction mixture to reach neutral pH 6-7, stir it well. The mixture with 2-bromo-4'-methylpropiophenone is filtered through a Buchner funnel. Product is washed with small amount of distilled water.
12. Crude 2-bromo-4'-methylpropiophenone (cas 1451-82-7) is used for further reactions. Theoretical yield up to 1530 g. Practice yield is almost quantitative (video yield 94%).

13. The resulting product is left in the reactor.

Stage 2. Methamination.
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1. Ethyl acetate 6 l is poured into the reactor.
2. Reaction mixture is stirred and heated in Jacketed reactor up to 30 °C with help of heating system.
3. The mixture is stirred until complete amount of 2-bromo-4'-methylpropiophenone (cas 1451-82-7) is dissolved.
4. Methylamine 40% aq 2 l is added at once.
5. The mixture is stirred for 20 min, temperature is kept below 65 °C.
6. The stirring is stopped. The reaction mixture is left for layer separations. A bottom layer is drained through a bottom reactor tap..
7. After that, the mixture is heated up to 55 °C and reactor vacuum pump is turned on. The reactor condenser chiller pump is turned on as well.
8. All amount of ethyl acetate or the biggest part of it is distilled off.
9. Vacuum pump is turned off. Acetone is added to the reactor with a constant stirring.
10. Hydrochloric acid (500 ml) is placed into the drip funnel and the funnel is installed onto the reactor neck.
11. Hydrochloric acid is added dropwise to reach pH 5 with constant stirring. A small amount (~2-5 ml) of reaction mixture is drained from the bottom reactor tap in order to check pH by pH indicator stripe. The sample is poured back into the reaction mixture.
12. After that, the mixture is poured into a bucket and the bucket is put into a freezer for 12 h.


Download Video

Stage 3. Filtration.
1. A vacuum filtration system (Nutsche filter, filter cloth, vacuum pump) is assembled and installed.
2. The vacuum pump is turned on.
3. A bucket content from step 13 stage 2 is poured to the
Nutsche filter.
4. The mixture is filtered and pressed until the funnel content is become solid.
5. A cold dry acetone is poured onto the solid product in the funnel in several small portions during filtration.
6. Acetone is filtered. Step 5 is repeated, if the solid is not white.
7. White solid 4-MMC product is moved into a Pyrex dish for a drying after filtration procedure.
8. Pyrex dish with 4-MMC is placed into a dry well ventilated warm room.
9. 4-MMC product is dried to a constant mass. Product is mixed and grinded periodically in order to increase drying speed.


Stage 4. Recrystallisation.
Mephedrone (4MMC) crystallization
 
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woohoo

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Kas seda ei peaks eraldama n-metüülatsetamiidist?
Tundub selle räpane reaktsioon, kui palju see annab võrreldes nmp või aromaatse lahustiga?
 

yin-yang

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N-metüülatsetamiid peaks lahustuma atsetoonis, kuigi ma ei leidnud, kui palju. Freebase on tõepoolest must ja saadud pulber muutub kristalliseeruva lahustisegu lisamisel roheliseks (reageerimata ketoon?). Tema kindel oletada, et see ei ole kõige puhtam protseduur.

Mõned vanduvad, et mis tahes muu reaktsioon peale selle, mis kasutab NMP-d lahustina, annab palju, palju kehvema tulemuse lõpptootes. Rohkem kiiret kõrvetust ilma eufooriata.

Kas sa käivitasid GC-MS-i, et näha, kas saadud pulbris / kristallides on lisandeid?
@G.Patton
@Marvin "Popcorn" Sutton
@William Dampier
 

G.Patton

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Tere, ilmselt tegite midagi valesti või teie reagendid ei ole nii head. Jah, me tegime GC-MS-i. 96,4% 4-MMC
PwIN6e4125
 

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yin-yang

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Ma ei ole seda reaktsiooni veel proovinud. Vaatasin siin avaldatud videot jood-ketooni aminatsioon. Seal nägin, et freebase on must ja pulber muutis kristalliseerumiseks ettevalmistamisel värvi. Võib-olla oli see must, sest jood on lahkuv rühm, erinevalt broomist.
Küsimused kinnitada:

1. Ülaltoodud tulemused on etüülatsetaadist kui lahustist ?
2. Kas olete teinud seda reaktsiooni EA ja bromoketooniga, kas freebase näeb teisiti välja?
3. Märkasin videost, et EA-st saadud kristallid näevad välja nagu klaas, samas kui NMP on palju valgemad. Ma lugesin teie postitust 4-MMC stereokeemia kohta, kuidas S ja R enantiomeerid moodustavad erineva välimusega kristallid, kas mõlemad kristallid on võrdselt raseemilised?
4. Kas te märkasite mingit erinevust EA ja näiteks NMP subjektiivses mõjus lõpptootes?

Tänan teid nende tulemuste avaldamise eest.
 

DavidNichols

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Kas te saaksite mulle selle postituse lingi anda?
 

G.Patton

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Tegelikult ma ei mäleta täpselt. Tõenäoliselt jah.
Jah, need on raseemilised kristallid.
Ma ei ole toodet maitsnud nagu iga hea veinitootja =)
 

StarWars

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8. Pärast seda kuumutatakse segu kuni 55
videos on selgelt öeldud, et ei ole vaja kuumutada. ja siin keegi kirjutas, et siis kuumutada, mis siis, kui segu ise saavutab temperatuuri mitte kõrgemal kui 65 °.
 

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G.Patton

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Tere, 55 kraadi *C on vaja lahustite ja metüülamiini üleliigseks vaakumiga aurustumiseks. See on vabatahtlik protseduur.
4d1MKgRTyH
 

goku1008

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can i skip this i dont have vacuum systume
and plz give me your screenshot video link plz
 

G.Patton

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This video in the topic, dude...
Yes, you can separate layers without vacuum. There is this information in the screenshot.
 

Chemix-Express

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Olen selle sünteesi suhtes väga uudishimulik, mõne päeva pärast on mul võimalus seda katsetada, seega on mul mõned küsimused:
1. Kas 2. sammu punktis 10 võib atsetooni asemel kasutada IPA-d? Kui ma kasutan HCL 35-37% aq koos atsetooniga, on alati palju värvi, 1,4-dioksaan aitas, kuid on väga kallis. Kas te arvate, et IPA töötab?
2. 2. etapis, punktis 5 öeldakse, et kogu m40 tuleb lisada korraga, samas kui punktis 6 öeldakse, et temperatuur peab olema alla 65 kraadi C. Kas ma saan temperatuuri kontrollida m40 järk-järgult lisades või tingimata välise külmkapi abil?
3. Kas ma peaksin arvestama reaktsiooniaega (20 minutit) alates hetkest, mil ma lõpetan m40 lisamise?
4. Mind huvitab, miks on nii vähe teavet 4MMC sünteesi kohta etüülatsetaadis, kui ei alguses ega reaktsiooni ajal ei pea segu kuumutama ja etüülatsetaat ise on väga odav. Kas sellele järgneb reaktsiooni madal saagis/puhtus?
5. Kas lühidalt öeldes oleks suhe 1kg bk4, 2L m40, 2L etüülatsetaat hea või on parem anda 1,5L m40 ja 2,5L etüülatsetaati iga kg bk4 kohta?
 

little-flower

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Kas me saame selle reaktsiooni teostada 12% H202-ga? Ma arvan, et võib-olla on see hea""
 

StarWars

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U saab teha
 

Rush-Benzo

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Kasutades valmis BK4, kui palju peaksin andma seda 2L m40 jaoks?
 

G.Patton

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Rush-Benzo

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Ma viitasin millelegi täiesti erinevale. Ma ei tea, kui palju lõplik BK4 teil pärast 1. etapi lõpetamist välja tuli. Ma tahan alustada 2. etapist ja ma ei tea, kui palju BK4 kasutada. Kui palju teil lõplikult tuli välja 1. etapist.
 

G.Patton

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Umbes 1350-1450 g 2-bromo-4'-metüülpropiofenooni esimesest etapist.
 

Rush-Benzo

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Tänan teid väga.

Kui see ei ole probleem, esitan veel ühe küsimuse. Sammu 2 punktis 9 ütlete, et destilleerida vähemalt pool etüülatsetaadist, mida see peaks tegema? Õppevideos on öeldud, et see samm on vabatahtlik. Kui ma selle ära jätan, kas ma kaotan tõhusust, kvaliteeti või on mul lihtsalt lihtsam töötada väiksema mahuga vedelikuga?

Olen ostmas võimsat vaakumpumpa, uudishimust küsin, kui kaua võtab nende 6L etüülatsetaadi destilleerimine 55 kraadini kuumutades aega?
 

StarWars

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Vaadake videot, kui u kasutate 1kg bk4 u vajate 2l etüülatsetaati ja 2l metüülamiini.
Seal nad müüvad 6 l videol haha
 

G.Patton

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>>> 2. sammu punktis 9 öeldakse, et vähemalt pool etüülatsetaadist tuleb destilleerida, mida see peaks tegema?
See on vajalik teie mefedrooni kristalliseerimiseks.
>>> Kas ma kaotan selle ärajätmisega tõhusust, kvaliteeti või hõlbustab see lihtsalt tööd väiksema mahuga vedelikuga?
Te destilleerite seda igal juhul, see on parem teha selles etapis, et saada suurem saagis HCl lisamise ajal.
 

StarWars

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paned selle elektripliidi peale ja pärast pesemist aurustub 50% lahustist aga selles videos on ikka palju vigu. puhastad 1x vesi + sooda siis 3 korda vesi siis aurustad 50% siis lisad magneesiumisoolfaati et mitte kaotada toodet ja hapestada ja see on kõik. Mul on sarnane video vanal sülearvutil kus nad kasutavad dcm asemel etüülatsetaati. Minu arvates ei ole mõtet aurustada, ma tegin ilma selleta ja mingeid probleeme sünteesi käigus ei tekkinud.
 
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