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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 590758Erstellt: 25. Oktober 2026

Water → Benzyl 3-allyl-4-oxocyclopentylcarbamate

https://huagongshe.com/reaction/590758

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktBenzyl carbamateHCID 12136—
EduktBismuth nitrate pentahydrateHCID 160911—
Edukt5-(Prop-2-en-1-yl)cyclopent-2-en-1-oneHCID 13444545—
LösungsmittelDichloromethaneHCID 6344—
ProduktBenzyl 3-allyl-4-oxocyclopentylcarbamateHCID 67513633—

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09233985B2
Quelldatensatzuspto-grants-2016_01
ORD IDord-dbe0b42c5a31407dbb8d7d6ed01b87d4
Quellennotizuspto-grants-2016_01