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HRID 1873519생성일: 2026년 10월 25일

1-Butanol → 5-Cyano-hexahydro-cyclopenta[c]pyrrole-2-carboxylic acid dimethylamide

https://huagongshe.com/reaction/1873519

반응식

참여 물질

역할이름HCID투입량
반응물1-ButanolHCID 263—
반응물Tosylmethyl isocyanideHCID 161915—
반응물Potassium tert-butoxideHCID 23665647—
반응물N,N-Dimethyl-5-oxo-hexahydrocyclopenta[c]pyrrole-2(1H)-carboxamideHCID 59151531—
용매WaterHCID 962—
용매1,2-DimethoxyethaneHCID 8071—
용매Sodium chloride; waterHCID 57417360—
생성물5-Cyano-hexahydro-cyclopenta[c]pyrrole-2-carboxylic acid dimethylamideHCID 6862619151.2%

반응 단계

N,N-dimethyl-5-oxo-hexahydro-cyclopenta[c]pyrrole-2-carboxamide 1g (12.9 g, 0.066 mol) and 4-toluenesulfonylmethyl isocyanide (14.2 g, 0.0727 mol) were dissolved in 240 mL of 1,2-dimethoxyethane with stirring upon cooling by an ice-water bath, followed by dropwise addition of a solution of potassium tert-butoxide (14.8 g, 0.132 mol) in tent-butanol. Upon completion of the addition, the ice-water bath was removed. The reaction mixture was warmed up to room temperature and reacted overnight. The reaction was monitored by TLC until the disappearance of the starting materials. The mixture was diluted with 100 mL of water and 50 mL of saturated brine and extracted with ethyl acetate (200 mL×3). The combined organic extracts were dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography to obtain the title compound 5-cyano-hexahydro-cyclopenta[c]pyrrole-2-carboxylic acid dimethylamide 12a (7.0 g, yield 51%) as a light yellow oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08304411B2
출처 데이터셋uspto-grants-2012_11
ORD IDord-5e5a9fc38f4b49d98e47f65eb2cea8d3
출처 메모uspto-grants-2012_11