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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1030149생성일: 2026년 10월 26일

Acetic Acid → (3S)-3-(4-Methoxybenzylthio)-1-methylpyrrolidine

https://huagongshe.com/reaction/1030149

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물FormaldehydeHCID 712—
반응물Ethyl AcetateHCID 8857—
반응물(3S)-3-(4-methoxybenzylthio)pyrrolidineHCID 14880282—
용매WaterHCID 962—
용매AcetonitrileHCID 6342—
생성물(3S)-3-(4-Methoxybenzylthio)-1-methylpyrrolidineHCID 57243155—

반응 단계

750 mg of (3S)-3-(4-methoxybenzylthio)pyrrolidine [which had been prepared by neutralization of 900 mg of (3S)-3-(4-methoxybenzylthio)pyrrolidine hydrochloride, prepared as described in step (3) above, with sodium bicarbonate] were dissolved in 15 ml of dry acetonitrile, and 1.44 ml of a 35% by volume solution of formaldehyde in water was added to the solution. The reaction mixture was then stirred for 15 minutes, after which it was neutralized by the addition of acetic acid; it was then again stirred for a further 2.5 hours. At the end of this time, the reaction mixture was poured into 200 ml of ethyl acetate, and the mixture was washed with a 2N aqueous solution of potassium hydroxide and an aqueous solution of sodium chloride. The organic layer was dried over potassium carbonate and the solvent was distilled off under reduced pressure. The residue was purified by column chromatography through silica gel (eluted with a 3:1 by volume mixture of ethyl acetate and methanol), to afford 349 mg of the title compound as a colorless oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05104867
출처 데이터셋uspto-grants-1992_04
ORD IDord-15ea8125c7bd4efcb6fbffe313c03027
출처 메모uspto-grants-1992_04