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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1457733생성일: 2026년 10월 25일

Benzyl Alcohol → (2RS,3SR)-2-benzyloxycarbonyl-5-oxotetrahydrofuran-3-carboxylic acid

https://huagongshe.com/reaction/1457733

반응식

참여 물질

역할이름HCID투입량
반응물Benzyl AlcoholHCID 244—
반응물DicyclohexylcarbodiimideHCID 10868—
반응물Tetrahydro-5-oxofuran-2,3-dicarboxylic acidHCID 98259—
용매AcetoneHCID 180—
생성물(2RS,3SR)-2-benzyloxycarbonyl-5-oxotetrahydrofuran-3-carboxylic acidHCID 18705291—

반응 단계

5.3 g of (2RS,3SR)-5-oxotetrahydrofuran-2,3-dicarboxylic acid was dissolved in 90 ml of acetone, and 6.6 g of N,N'-dicyclohexylcarbodiimide was added thereto, followed by stirring at room temperature for 2.5 hours. 3.3 ml of benzyl alcohol was added to the reaction solution, followed by stirring at the same temperature for 2 days. Insoluble matters were filtered off, and then the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate=4/1→chloroform/methanol=50/1) to obtain 6.55 g of the above-identified compound as a yellow solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05849747
출처 데이터셋uspto-grants-1998_12
ORD IDord-650808c48dbc4979a22dd0e9a62a951d
출처 메모uspto-grants-1998_12