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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2050186생성일: 2026년 10월 26일

Dichloromethane → 1-Benzylpyrrolidine-3-carbaldehyde

https://huagongshe.com/reaction/2050186

반응식

참여 물질

역할이름HCID투입량
반응물DichloromethaneHCID 6344—
반응물DicyclohexylcarbodiimideHCID 10868—
반응물Phosphorus pentachlorideHCID 24819—
반응물(1-Benzylpyrrolidin-3-yl)methanolHCID 5176654—
용매Dimethyl SulfoxideHCID 679—
생성물1-Benzylpyrrolidine-3-carbaldehydeHCID 458947866%

반응 단계

To a solution of 61.8 g (0.3 mole) of dicyclohexylcarbodiimide in 400 ml of dry dimethylsulfoxide is dropwise added a solution of 19.10 g (0.1 mole) of 1-benzyl-3-hydroxymethylpyrrolidine [prepared in the manner described in J. O. C. 26, 1519 (1961) by YAO-HUA WU and R. F Feldkamp] under ice-cooling for 15 minutes, and the mixture is stirred at room temperature overnight. Dicyclohexylcarbodiimide (13.26 g; 60 mmoles) and phosphorus pentachloride (4.40 g; 30 mmoles) are added thereto and the mixture is stirred overnight, poured into ice water, mixed with 300 ml of methylene chloride and stirred for 30 minutes. The insoluble materials, which appear, are filtered off and washed with water. The combined filtrate and washings are washed twice with 200 ml of methylene chloride, adjusted to pH 9 with 20 (w/w) % aqueous sodium carbonate solution, and extracted four times with 200 ml of methylene chloride. The extract is washed with 20 (w/w) % aqueous sodium hydrogensulfite solution. The aqueous layer is separated, washed thrice with 100 ml of methylene chloride, mixed with 20 (w/w) % aqueous sodium carbonate solution, and extracted with methylene chloride. The extract is washed with water, dried over sodium sulfate and evaporated under reduced pressure to yield crude oily 1-benzyl-3-formylpyrrolidine in 66% yield.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04200628
출처 데이터셋uspto-grants-1980_04
ORD IDord-39fcd3c9ac6b4bf2ae7f201216d33f9d
출처 메모uspto-grants-1980_04