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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2280698Generated: October 25, 2026

Benzyl carbamate → HCID 25260225, compound

https://huagongshe.com/reaction/2280698

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl carbamateHCID 12136—
ReactantBismuth nitrate pentahydrateHCID 160911—
Reactant3,6-dihydro-2H-pyran-3-oneHCID 4672596—
SolventDichloromethaneHCID 6344—
ProductHCID 25260225HCID 2526022573.5%

Reaction Steps

2H-pyran-3(6H)-one (2.33 g, 23.75 mmol), benzyl carbamate (4.31 g, 28.5 mmol), and DCM (2.375 mL) were added to a small vial and stirred vigorously. To the thick syrup was added bismuth(III) nitrate pentahydrate (1.728 g, 3.56 mmol). The vial was capped and the reaction was stirred vigorously overnight. The reaction was diluted with DCM and filtered through a pad of celite. The filtrate was condensed and purified on a 100G SNAP Biotage column (10-100% ethyl acetate in hexane) to give benzyl 5-oxotetrahydro-2H-pyran-3-ylcarbamate (4.35 g, 17.45 mmol, 73.5% yield) as a pale yellow oil; 1H NMR (400 MHz, CDCl3) δ ppm 7.28-7.41 (m, 5H), 5.20-5.28 (m, 1H), 5.05-5.15 (m, 2H), 4.24-4.35 (m, 1H), 4.01-4.06 (m, 1H), 3.89-3.95 (m, 1H), 3.80-3.87 (m, 1H), 2.73 (d, J=5.47 Hz, 1H), 2.64-2.71 (m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09139534B2
Source datasetuspto-grants-2015_09
ORD IDord-45bac57ddec846539113dd5d9e70d1d7
Source noteuspto-grants-2015_09