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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 358881생성일: 2026년 10월 27일

Water → tert-Butyl 6-Oxa-3-azabicyclo(3.1.0)hexane-3-carboxylate

https://huagongshe.com/reaction/358881

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물m-Chloroperbenzoic acidHCID 70297—
반응물tert-Butyl 2,5-dihydro-1H-pyrrole-1-carboxylateHCID 5148195—
용매ChloroformHCID 6212—
생성물tert-Butyl 6-Oxa-3-azabicyclo(3.1.0)hexane-3-carboxylateHCID 1010388058.8%

반응 단계

2.96 g (0.012 mole) of 70% aqueous m-chloroperbenzoic acid were added to a solution of 1.69 g (0.01 mole) of 1-t-butoxycarbonyl-3-pyrroline [prepared as described in Step (a) above] in 10 ml of chloroform, whilst ice-cooling, and the mixture was stirred with ice-cooling for 8 hours and then with water-cooling for 15 hours. At the end of this time, the reaction mixture was extracted with toluene and the extract was washed, in turn, with an aqueous solution of sodium bicarbonate, a 0.1N aqueous solution of sodium thiosulfate and water. It was then dried over anhydrous sodium sulfate, and the solvent was removed by evaporation under reduced pressure. The residue was subjected to silica gel column chromatography eluted with a 1:5 by volume mixture of ethyl acetate and toluene, to afford 1.09 g of 1-t-butoxycarbonyl-3,4-epoxypyrrolidine as a colorless oily substance.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04997943
출처 데이터셋uspto-grants-1991_03
ORD IDord-3b5843a477ee452f954ed9e0b498034d
출처 메모uspto-grants-1991_03