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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 475733Generated: October 26, 2026

Isocyanatocarbonyl chloride → 7-phenyl-6,7-dihydrocyclopenta[e][1,3]oxazine-2,4(3H,5H)-dione

https://huagongshe.com/reaction/475733

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsocyanatocarbonyl chlorideHCID 119708—
Reactant2-PhenylcyclopentanoneHCID 290154—
SolventEthyl AcetateHCID 8857—
SolventSodium BicarbonateHCID 516892—
Product7-phenyl-6,7-dihydrocyclopenta[e][1,3]oxazine-2,4(3H,5H)-dioneHCID 1053736213.1%

Reaction Steps

A solution of 2-phenylcyclopentanone (19.995 g, 125 mmol) and N-(chlorocarbonyl)isocyanate (23.70 g, 225 mmol) was stirred at 58° C. for 1 h and at 130° C. for 45 min. The resulting tarrified reaction mixture was dissolved in ethyl acetate and neutralized with saturated aqueous sodium bicarbonate solution. The organic layer was dried over anhydrous magnesium sulfate and filtered. The product was purified by column chromatography on silica gel to give 7-phenyl-6,7-dihydrocyclopenta[e][1,3]oxazine-2,4(3H,5H)-dione (3.751 g, 16.36 mmol, 13% yield) as brownish solid. LC-MS (M+H)+=230.0. 1H NMR (500 MHz, CDCl3) δ ppm 8.34 (1H, br s), 7.35 (2H, t, J=7.3 Hz), 7.27-7.32 (1H, m), 7.18 (2H, d, J=7.3 Hz), 4.20 (1H, t, J=7.6 Hz), 2.82-2.91 (1H, m), 2.61-2.79 (2H, m), 2.11-2.21 (1H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08637525B2
Source datasetuspto-grants-2014_01
ORD IDord-f50b6101f216415ba202f7c3750512f4
Source noteuspto-grants-2014_01