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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 61413생성일: 2026년 10월 23일

Water → Benzyl 3-allyl-4-oxocyclopentylcarbamate

https://huagongshe.com/ko/reaction/61413

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Benzyl carbamateHCID 12136—
반응물Bismuth nitrate pentahydrateHCID 160911—
반응물5-(Prop-2-en-1-yl)cyclopent-2-en-1-oneHCID 13444545—
용매DichloromethaneHCID 6344—
생성물Benzyl 3-allyl-4-oxocyclopentylcarbamateHCID 67513633—

반응 단계

A solution of 5-(propene-3-yl)cyclopent-2-enone (4.28 g, 35 mmol) in dichloromethane (15 mL) was treated with benzyl carbamate (10.6 g, 70 mmol) and bismuth trinitrate pentahydrate (2.2 g, 4.5 mmol), stirred rapidly for 18 h, then diluted with dichloromethane (50 mL). The mixture was filtered through Celite® (rinse with dichloromethane) and the filtrate added directly to a silica gel column (˜550 cc). Elution first with 3:2 petroleum ether/dichloromethane afforded recovered starting material (1.01 g), then 4:1 heptane/ethyl acetate gave the subject compound (4.54 g, 47.5% uncorrected yield) as a pale yellow oil. NMR (CDCl3): δ 7.28 (br s, 5 H), 5.55-5.70 (m, 1 H), 5.03 (br s, 2 H), 4.90-5.10 (m, 2 H), 4.75-4.90 (m, 1 H), 4.10-4.30 (m, 1 H), 2.40-2.80 (m, 2 H), 2.15-2.40 (m, 2 H), 1.85-2.15 (m, 3 H). MS (M+Na): 296.0; MS (M−H2O+1): 256.0 (no M+1 visible).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09440995B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-f2d56955c2bc4d60b6aa20377463e990
출처 메모uspto-grants-2016_09