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-- Ingredients and Method to making scones?
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Ingredients and Method to making scones?
i was just wondering if anyone had the list of ingredients, and a method for concocting cherry scones
time to start putting that cooking practice into practice hehe 
first u need 200g of don't be stupid
and 300g of my full postal address with a stamped addressed envelope 
lol its for erm, research, yes thats right, research purposes only 
u wuss, make it and get spannered 
To a well stirred, cooled mixture of 34g of 30% H202 (hydrogen peroxide) in 150g 80% HCO2H (formic acid) there was added, dropwise, a solution of 32.4g isosafrole in 120ml acetone at a rate that kept the reaction mixture from exceeding 40 deg C. This required a bit over 1 hour, and external cooling was used as necessary. Stirring was continued for 16 hours, and care was taken that the slow exothermic reaction did not cause excess heating. An external bath with running water worked well. During this time the solution progressed from an orange color to a deep red. All volatile components were removed under vacuum which yielded some 60g of a very deep residue. This was dissolved in 60ml of MeOH (methyl alcohol -- methanol), treated with 360ml of 15% H2SO4 (sulfuric acid), and heated for 3 hours on the steam bath. After cooling the mixture was extracted with 3x75ml Et2O (diethyl ether) or C6H6 (benzene). Its recommended that, the pooled extracts can washed -- first with H2O and then with dilute NaOH (sodium hydroxide). Then the solvent is removed under vacuum to afford 20.6g 3,4-methylenedioxyphenylacetone (3,4-methylenedioxybenzyl methyl ketone). The final residue may be distilled at 2.0mm/108-112 deg C, or at about 160 deg C at the water pump.
Add 23g 3,4-methylenedioxyphenylacetone to 65g HCONH2 (formamide) and heat at 190 deg for five hours. Cool, add 100ml H20, extract with C6H6 (benzene) and evaporate in vacuum the extract. Add 8ml MeOH (methyl alcohol -- methanol) and 75ml 15% HCl to residue, heat on water bath two hours and extract in vacuum (or basify with KOH and extract the oil with benzene and dry, evaporate in vacuum) to get 11.7 g 3,4-methylenedioxyamphetamine (MDA).
To produce MDMA substitute N-methylformamide for formamide in the above synthesis.
unless your a fully qualified chemist i seriously don't think you should bother risking your life or that of any of your friends
well when someone gives me the list i'll have to incorporate a bit of , erm, subject testing into my erm, project, lol.
hmmm, my own concotion of 110mg mdma pills yummy 
Why bother? These things only cost 1,5 Euro each in Holland 
i am reporting this thread to a moderator.
| quote: |
| Originally posted by jploveparade To a well stirred, cooled mixture of 34g of 30% H202 (hydrogen peroxide) in 150g 80% HCO2H (formic acid) there was added, dropwise, a solution of 32.4g isosafrole in 120ml acetone at a rate that kept the reaction mixture from exceeding 40 deg C. This required a bit over 1 hour, and external cooling was used as necessary. Stirring was continued for 16 hours, and care was taken that the slow exothermic reaction did not cause excess heating. An external bath with running water worked well. During this time the solution progressed from an orange color to a deep red. All volatile components were removed under vacuum which yielded some 60g of a very deep residue. This was dissolved in 60ml of MeOH (methyl alcohol -- methanol), treated with 360ml of 15% H2SO4 (sulfuric acid), and heated for 3 hours on the steam bath. After cooling the mixture was extracted with 3x75ml Et2O (diethyl ether) or C6H6 (benzene). Its recommended that, the pooled extracts can washed -- first with H2O and then with dilute NaOH (sodium hydroxide). Then the solvent is removed under vacuum to afford 20.6g 3,4-methylenedioxyphenylacetone (3,4-methylenedioxybenzyl methyl ketone). The final residue may be distilled at 2.0mm/108-112 deg C, or at about 160 deg C at the water pump. Add 23g 3,4-methylenedioxyphenylacetone to 65g HCONH2 (formamide) and heat at 190 deg for five hours. Cool, add 100ml H20, extract with C6H6 (benzene) and evaporate in vacuum the extract. Add 8ml MeOH (methyl alcohol -- methanol) and 75ml 15% HCl to residue, heat on water bath two hours and extract in vacuum (or basify with KOH and extract the oil with benzene and dry, evaporate in vacuum) to get 11.7 g 3,4-methylenedioxyamphetamine (MDA). To produce MDMA substitute N-methylformamide for formamide in the above synthesis. |
| quote: |
| Originally posted by jploveparade Why bother? These things only cost 1,5 Euro each in Holland |
| quote: |
| Originally posted by dj_mdma i've already seen that, its not particularly clear on what equipment on what to use either. the chemicals involved are also quite difficult to make/obtain. and Dom i'm currently studying a degree in Pharmacology and have done A level Chemistry etc. and of course am mates with plenty of chemists |
If you wanna experiment, you should do so in the bedroom...
or bathroom...
kitchen...
in the car..
garden...
Got it?

| quote: |
| Originally posted by Dom fair enough but just remember the consequences if u made just one mistake...... |
LOL, im glad i live close to Lam, but i do feel a bit like a test bunny, id rather be a playboy bunny
once you have finished ur degree lam you will probably be able to do it.
a lot of the processes involve chemistry which is studied at degree level. 
the only thing a few of the ingrediants are a bit dangerous 
Grow some mushrooms instead maybe?
Crusader
* go lam, go lam, go go go!
waves pom poms
Can u stamp the TSN logo on em?
I want mine with plenty of vitamin c
Crusader
| quote: |
| Originally posted by dstrukt Can u stamp the TSN logo on em? |
hehe a nice bit of advertising that would be for The Beautiful system 
i was thinking about it and it would be so easy to do in my college, let alone my university lab!
edited ur first post + title.
u can understand y 
i like cherry scones
mmmm
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