돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 428128생성일: 2026년 10월 24일

Acetic Acid → N-Methylmescaline

https://huagongshe.com/ko/reaction/428128

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물Formic AcidHCID 284—
반응물MescalineHCID 4076—
반응물Acetic AnhydrideHCID 7918—
용매TetrahydrofuranHCID 8028—
생성물N-MethylmescalineHCID 138365—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06313153B1
출처 데이터셋uspto-grants-2001_11
ORD IDord-1863a5e191f34d89b721e8ec1a0740af
출처 메모uspto-grants-2001_11