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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1917330생성일: 2026년 10월 27일

Trifluoroacetic acid → rel-(3aR,6aR)-Methyl 2-benzylhexahydrocyclopenta[c]pyrrole-3a(1H)-carboxylate

https://huagongshe.com/reaction/1917330

반응식

참여 물질

역할이름HCID투입량
반응물Trifluoroacetic acidHCID 6422—
반응물Benzyl(methoxymethyl)((trimethylsilyl)methyl)amineHCID 353442—
반응물Methyl cyclopent-1-ene-1-carboxylateHCID 549129—
용매DichloromethaneHCID 6344—
생성물rel-(3aR,6aR)-Methyl 2-benzylhexahydrocyclopenta[c]pyrrole-3a(1H)-carboxylateHCID 151551483%

반응 단계

A catalytic amount of trifluoroacetic acid was added to a solution of 1-cyclopentene-1-carboxylic acid methyl ester (2.52 g, 20.0 mmol) and N-benzyl-N-(methoxymethyl)-N-trimethylsilylmethylamine (5.00 g, 21.1 mmol) in dichloromethane (40 mL) at room temperature, and the mixture was heated with stirring at room temperature for 15.5 hours. The reaction solution was diluted with dichloromethane (100 mL) and washed with a saturated sodium bicarbonate solution (80 mL). The washed aqueous layer was further extracted with dichloromethane (50 mL). The organic layers were combined and dried over anhydrous sodium sulfate. After filtration, the solvent was evaporated under reduced pressure. The resulting residue was purified by silica gel column chromatography (hexane:ethyl acetate=95:5→90:10→80:20) to give 4.28 g (83%) of the title compound as a colorless transparent oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08618094B2
출처 데이터셋uspto-grants-2013_12
ORD IDord-0be8207185c648c4ab86050b9ee72355
출처 메모uspto-grants-2013_12