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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1974177생성일: 2026년 10월 26일

Triethylamine → Methyl cis-1-(2,4-Dimethoxybenzyl)-3-phenoxyacetamido-4-oxo-2-azetidinecarboxylate

https://huagongshe.com/reaction/1974177

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Phenoxyacetyl chlorideHCID 69703—
반응물Methyl cis-1-(2,4-dimethoxybenzyl)-3-azido-4-oxoazetidine-2-carboxylateHCID 86734328—
반응물HCID 178418361HCID 178418361—
촉매PalladiumHCID 23938—
용매EthanolHCID 702—
용매Diethyl EtherHCID 3283—
용매DichloromethaneHCID 6344—
생성물Methyl cis-1-(2,4-Dimethoxybenzyl)-3-phenoxyacetamido-4-oxo-2-azetidinecarboxylateHCID 70577439—

반응 단계

A mixture containing 10.0 g (0.0312 mole) of methyl cis-3-azido-1-(2,4-dimethoxybenzyl)-4-oxoazetidine-2-carboxylate, 1.0 g of 10% palladium on carbon and 200 ml of ethanol was hydrogenated at 60 psi of hydrogen at 40°-45° for 2 hours. The reaction mixture was allowed to cool to 25° and was filtered through celite. After removing the solvents in vacuo there remained a clear, yellow gum. The crude amine was taken up in 100 ml of anhydrous methylene dichloride and was cooled to 0° in an ice bath. To this solution was added 4.32 ml (0.0312 mole) of triethylamine followed by the slow addition of a solution of 5.32 g (0.0312 mole) of phenoxyacetyl chloride in 40 ml of methylene dichloride. The mixture was stirred at 0° for 1 hour then extracted successively with water, aqueous hydrochloric acid, aqueous sodium bicarbonate and brine and was dried over anhydrous magnesium sulfate. Filtration followed by removal of the solvent in vacuo afforded a yellow solid. This material was partially dissolved in ether, cooled to -25° and filtered to give methyl cis-1-(2,4-dimethoxybenzyl)-4-oxo-3-phenoxyacetylaminoazetidine-2-carboxylate as a white solid; tlc: benzene:ethyl acetate (1:1), silica gel, Rf = 0.38; mp 115.5°-116.0° (ethyl acetate-hexane).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04000154
출처 데이터셋uspto-grants-1976_12
ORD IDord-66b1fb741ea14e949064ecebeed1fab1
출처 메모uspto-grants-1976_12