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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1029생성일: 2026년 10월 23일

Glycidol → p-(N-2,3-dihydroxypropylamino)benzonitrile

https://huagongshe.com/ko/reaction/1029

반응식

참여 물질

역할이름HCID투입량
반응물GlycidolHCID 11164—
반응물4-AminobenzonitrileHCID 13396—
반응물PhenolateHCID 119047—
반응물3-p-Cyanophenyl-5-methanesulfonyloxymethyloxazolidin-2-oneHCID 15281527—
용매DimethylformamideHCID 6228—
생성물p-(N-2,3-dihydroxypropylamino)benzonitrileHCID 10171309—

반응 단계

1 Equivalent of NaH is added to a solution of 1.7 g of Na p-methoxycarbonylmethylphenoxide (obtainable by converting p-hydroxybenzyl cyanide into the corresponding carboxylic acid, esterifying with methanol to give p-methoxycarbonylmethylphenol and subsequently converting the latter into the phenoxide) in 20 ml of dimethylformamide (DMF), and the mixture is stirred at room temperature for 30 min. After that, 3.0 g of 3-p-cyanophenyl-5-methanesulfonyloxymethyloxazolidin-2-one ("A") (obtainable by reacting p-aminobenzonitrile with 2,3-epoxypropan-1-ol to give p-(N-2,3-dihydroxypropylamino)benzonitrile, reacting the latter with diethyl carbonate in the presence of K tert-butoxide to give 3-p-cyanophenyl-5-hydroxymethyloxazolidin-2-one and subsequently esterifying the latter with methanesulfone chloride), dissolved in 10 ml of DMF, are added and the mixture is once again stirred at room temperature for 15 min. Following removal of the solvent, and the customary working-up, 3-p-cyanophenyl-5-(p-methoxycarbonylmethylphenoxymethyl)oxazolidin-2-one is obtained, M.p. 114°-115°.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05723480
출처 데이터셋uspto-grants-1998_03
ORD IDord-db32eb67f898496ca933619d4788c566
출처 메모uspto-grants-1998_03