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HRID 1719274생성일: 2026년 10월 27일

Isoamyl Nitrite → methyl 2-[(4R)-3-bromo-4-allyl-2-oxoazetidin-1-yl]-3-methyl-2-butenoate

https://huagongshe.com/reaction/1719274

반응식

참여 물질

역할이름HCID투입량
반응물Isoamyl NitriteHCID 8053—
반응물p-Toluenesulfonic acid monohydrateHCID 521998—
반응물Triethylammonium bromideHCID 2734074—
반응물HCID 54087051HCID 54087051—
용매DichloromethaneHCID 6344—
생성물methyl 2-[(4R)-3-bromo-4-allyl-2-oxoazetidin-1-yl]-3-methyl-2-butenoateHCID 5433133581.3%

반응 조건

온도0 °C

반응 단계

A mixture of methyl 2-[(4R)-3-amino-4-allyl-2-oxoazetidin-1-yl]-3-methyl-2-butenoate (815 mg), triethylamine hydrobromide (2.50 g) and p-toluenesulfonic acid hydrate (1.17 g) in methylene chloride (30 ml) was cooled to 0° C. and isopentyl nitrite (0.54 ml) was added. After stirring for 20 minutes at the same temperature, the mixture was concentrated and the residue was dissolved in ethyl acetate (50 ml). The solution was washed successively with 10% aqueous sodium bisulfite, water and brine, dried over magnesium sulfate and evaporated to give methyl 2-[(4R)-3-bromo-4-allyl-2-oxoazetidin-1-yl]-3-methyl-2-butenoate (840 mg) as a crude oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04539152
출처 데이터셋uspto-grants-1985_09
ORD IDord-d115d52a53914b2a9b8b5a416045f907
출처 메모uspto-grants-1985_09