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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 432575생성일: 2026년 10월 24일

1-(Trimethylsilyl)pyrrolidin-2-one → 3-(2-Chloropyrid 5-yl-methyl)-pyrrolid-2-one

https://huagongshe.com/ko/reaction/432575

반응식

참여 물질

역할이름HCID투입량
반응물1-(Trimethylsilyl)pyrrolidin-2-oneHCID 84461—
반응물2-Chloro-5-(chloromethyl)pyridineHCID 155479—
반응물Lithium diisopropylamideHCID 2724682—
용매TetrahydrofuranHCID 8028—
용매CyclohexaneHCID 8078—
생성물3-(2-Chloropyrid 5-yl-methyl)-pyrrolid-2-oneHCID 18759788—

반응 단계

Under a nitrogen atmosphere at a temperature of from −78° C. to −60° C., 180 ml of a 1.5 molar solution of lithium diisopropylamide (IDA) in cyclohexane are added dropwise to 31.4 g of N-trimethylsilylpyrrolid-2-one in 150 ml of tetrahydrofuran (THF) and the reaction mixture is stirred at the same temperature for a further one hour. Then, at from −78° C. to −60° C., 25.5 g of 2-chloro-5-chloromethylpyridine in 40 ml of THF are added, and the mixture is stirred for a further 16 hours at that temperature and then for a further three hours at room temperature. The reaction mixture is poured onto a mixture of ice/water and extracted with ethyl acetate, and the organic phase is separated off The ethyl acetate phase is dried over sodium sulfate and concentrated to dryness by evaporation in vacuo. The residue is purified on silica gel using ethyl acetate/hexane (7:1) as eluant. The title compound having a melting point of 117-118° C. (compound 1.3) is obtained

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06664248B2
출처 데이터셋uspto-grants-2003_12
ORD IDord-dec8e6cd826940d6947cf8e1fe93d861
출처 메모uspto-grants-2003_12