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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 590758생성일: 2026년 10월 26일

Water → Benzyl 3-allyl-4-oxocyclopentylcarbamate

https://huagongshe.com/reaction/590758

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 번호US09233985B2
출처 데이터셋uspto-grants-2016_01
ORD IDord-dbe0b42c5a31407dbb8d7d6ed01b87d4
출처 메모uspto-grants-2016_01