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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 484681생성일: 2026년 10월 24일

2,6-Dimethoxybenzoyl chloride → (3S-trans)-3-[(2,6-dimethoxybenzoyl)amino]-4-methyl-1-[(phenylmethyl)oxy]-2-azetidinone

https://huagongshe.com/ko/reaction/484681

반응식

참여 물질

역할이름HCID투입량
반응물2,6-Dimethoxybenzoyl chlorideHCID 74810—
반응물ToluenesulfonateHCID 3424274—
반응물(3S-trans)-3-amino-4-methyl-1-(phenylmethoxy)-2-azetidinoneHCID 13036842—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매DichloromethaneHCID 6344—
생성물(3S-trans)-3-[(2,6-dimethoxybenzoyl)amino]-4-methyl-1-[(phenylmethyl)oxy]-2-azetidinoneHCID 13036849—

반응 단계

To a cold (-10° C.) solution of (3S-trans)-3-amino-4-methyl-1-(phenylmethoxy)-2-azetidinone, toluenesulfonate (0.95 g; see example 2D) in methylene chloride (50 ml) is added 2,6-dimethoxybenzoyl chloride (0.60 g) and 4-dimethylaminopyridine (0.61 g). The reaction is stirred under nitrogen and allowed to rise to 26° C. over five hours. The reaction mixture is concentrated to an oil and partitioned between ethyl acetate and aqueous hydrogen sulfate solution. The organic layer is washed with aqueous sodium bicarbonate, and brine, dried over sodium sulfate and concentrated to a foam (0.848 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04533660
출처 데이터셋uspto-grants-1985_08
ORD IDord-b3c4aefaa8124d5eaa3567e0899a03f9
출처 메모uspto-grants-1985_08