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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 474252Generated: October 26, 2026

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

https://huagongshe.com/reaction/474252

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 carbonisocyanatidic chloride (23.70 g, 225 mmol) was stirred at 58° C. for 1 h and at 130° C. for 45 min. The resulting tar 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 a 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 numberUS08637523B2
Source datasetuspto-grants-2014_01
ORD IDord-699f72df7ed549fcbde3232047a02321
Source noteuspto-grants-2014_01