Acetic Acid → N-Methylmescaline

A solution of the crude oil of 3,4,5-trimethoxy-phenethylamine in tetrahydrofuran (30 ml) was added to a mixed acid anhydride of acetic acid and formic acid, which had been synthesized by adding 98% formic acid (6.2 ml) to acetic anhydride (12.5 ml) under ice-cooling and reacting at 60° C. for 3 hours, under room temperature and stirred for 17 hours. The reaction mixture was concentrated under reduced pressure and tetrahydrofuran (40 ml) and borane-methyl sulfide complex (12 ml) were added to the residue under ice-cooling and stirring. The reaction mixture was heated and refluxed for 17 hours. After the reaction mixture was cooled, methanol was added to stop the reaction and concentrated under reduced pressure. A hydrogen chloride-methanol solution was added to the residue and heated and refluxed for 3 hours. The solvent was distilled out under reduced pressure and the residue was dissolved in 2N hydrochloric acid and washed with dichloromethane. The aqueous layer was made basic with sodium hydroxide and the released oil material was extracted with dichloromethane. After washed with water and dried over potassium carbonate, the solvent was distilled out under reduced pressure to yield N-methyl-3,4,5-trimethoxyphenethylamine (1.61 g) as a colorless oil.

1. customhad been synthesized
2. temperaturecooling
3. concentrationThe reaction mixture was concentrated under reduced pressure and tetrahydrofuran (40 ml) and borane-methyl sulfide complex (12 ml)
4. additionwere added to the residue under ice-
5. temperaturecooling
6. stirringstirring
7. temperatureThe reaction mixture was heated
8. temperaturerefluxed for 17 hours
9. temperatureAfter the reaction mixture was cooled
10. additionmethanol was added
11. customthe reaction
12. concentrationconcentrated under reduced pressure
13. additionA hydrogen chloride-methanol solution was added to the residue
14. temperatureheated
15. temperaturerefluxed for 3 hours
16. distillationThe solvent was distilled out under reduced pressure
17. dissolutionthe residue was dissolved in 2N hydrochloric acid
18. washwashed with dichloromethane
19. extractionthe released oil material was extracted with dichloromethane
20. washAfter washed with water
21. dry with materialdried over potassium carbonate
22. distillationthe solvent was distilled out under reduced pressure

ORD-Eintrag

ord-1863a5e191f34d89b721e8ec1a0740af

Quelldatensatz

uspto-grants-2001_11

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US06313153B1