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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 616157생성일: 2026년 10월 24일

Sodium Phosphate, Dibasic → Methyl cis-3-t-butoxycarbonylamino-4-oxoazetidine-2-carboxylate

https://huagongshe.com/ko/reaction/616157

반응식

참여 물질

역할이름HCID투입량
반응물Sodium Phosphate, DibasicHCID 24203—
반응물Potassium PersulfateHCID 24412—
반응물Methyl 3-t-butoxycarbonylamino-1-(2,4-dimethoxybenzyl)-4-oxoazetidine-2-carboxylateHCID 23470103—
용매WaterHCID 962—
용매AcetonitrileHCID 6342—
생성물Methyl cis-3-t-butoxycarbonylamino-4-oxoazetidine-2-carboxylateHCID 7042837231%

반응 단계

A solution of 10.5 g (26.7 mmole) of methyl 3-t-butoxycarbonylamino-1-(2,4-dimethoxybenzyl)-4-oxoazetidine-2-carboxylate in 500 ml of acetonitrile is degassed with argon and warmed to 80°. A degassed solution of 15 g (55.5 mmole) of potassium persulfate and 7.5 g (28 mmole) of sodium monohydrogen phosphate in 150 ml of water is added in five portions over 1 hr. The reaction is stirred at 80°-85° under argon for 2-3 hrs until all starting material is consumed (tlc). The reaction mixture is cooled, concentrated in vacuum, shaken with ethyl acetatewater. The organic phase is washed with dilute HCl, NaHCO3 solution and brine; dried over magnesium sulfate and evaporated to dryness. The residue is chromatographed over silica gel with 1:1 benzene-ethyl acetate to afford pure product which crystallized from ethyl acetate-hexane to yield 2.0 g (31%) of the title compound. A less pure fraction from the column, is crystallized from ethyl acetate-hexane to give an additional 0.5 g of product, overall yield, 38%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04072674
출처 데이터셋uspto-grants-1978_02
ORD IDord-d504fd3780a844abb0c2b5ea5e1cea0d
출처 메모uspto-grants-1978_02