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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 247702생성일: 2026년 10월 23일

Hydrochloric Acid → 1-Benzyl-4-ethynyl-3-(1-hydroxyethyl)-2-azetidinone

https://huagongshe.com/ko/reaction/247702

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물TriphenylphosphineHCID 11776—
반응물Potassium HydroxideHCID 14797—
반응물2,2'-Dipyridyl disulfideHCID 65093—
반응물3-Benzylamino-2-(1-hydroxyethyl)-5-trimethylsilyl-4-pentinic acid phenylthio esterHCID 54532351—
용매AcetonitrileHCID 6342—
용매TetrahydrofuranHCID 8028—
생성물1-Benzyl-4-ethynyl-3-(1-hydroxyethyl)-2-azetidinoneHCID 13959561—

반응 단계

There was dissolved 2.054 g (5.0 mmol) of 3-benzylamino-2-(1-hydroxyethyl)-5-trimethylsilyl-4-pentinic acid phenylthioester in 40 ml of THF, to which 3 ml of 4 N potassium hydroxide was added and the mixture was stirred at room temperature for 3 hours. The reaction mixture was neutralized with 2 N hydrochloric acid and was extracted six times with ethyl acetate while conducting salting-out. The extract was dried with anhydrous magnesium sulfate and concentrated. There was added 250 ml of acetonitrile to the concentrated solution, and then 1.57 g (60 mmol) of triphenylphosphine was added, to which 1.32 g (6.0 mmol) of 2,2'-dipyridyldisulfide in 50 ml of acetonitrile was added dropwise for 40 minutes while vigorously stirring with heating under reflux. After the solution was further heated under reflux for 1 hour, the obtained reaction mixture was concentrated, followed by purification with 50 g of silica-gel column-chromatography (eluent; methylene chloride→diethyl ether) and then with 50 g of silica-gel column-chromatography (eluent;hexane:diethyl ether=1:4) to give 801 mg of a trans-form and 62 mg of a cis-form of 1-benzyl-4-ethynyl-3-(1-hydroxyethyl)-2-azetidinone.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04709064
출처 데이터셋uspto-grants-1987_11
ORD IDord-74f19f2684e14a59a7a5c52e15c17844
출처 메모uspto-grants-1987_11