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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 475793Generated: October 30, 2026

Isocyanatocarbonyl chloride → HCID 58075467, compound

https://huagongshe.com/reaction/475793

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsocyanatocarbonyl chlorideHCID 119708—
Reactant2-(3,4-Difluorophenyl)cyclopentanoneHCID 62802355—
SolventEthyl AcetateHCID 8857—
ProductHCID 58075467HCID 5807546751.8%

Reaction Conditions

Temperature130 °C

Reaction Steps

A solution of 2-(3,4-difluorophenyl)cyclopentanone, (prepared in the manner of Intermediate P(1) and P(2)) (1.5 g, 7.65 mmol) and carbonisocyanatidic chloride (1.129 g, 10.70 mmol) was stirred at 58° C. in a high-pressure vessel for 1 h. The temperature was raised to 130° C. and the reaction mixture was stirred for an additional 2 h. After cooling to rt, the reaction mixture solidified. The solid residue was dissolved in ethyl acetate and washed with saturated aqueous solution of sodium bicarbonate. The organic layer was separated and the aqueous layer was extracted twice with ethyl acetate. The combined organic extracts were dried over anhydrous sodium sulfate and filtered. The solvent was removed in vacuum and the oily residue was purified by column chromatography on silica gel to provide 7-(3,4-difluorophenyl)-6,7-dihydrocyclopenta[e][1,3]oxazine-2,4(3H,5H)-dione (1.05 g, 3.96 mmol, 51.8% yield) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08637525B2
Source datasetuspto-grants-2014_01
ORD IDord-ff10c0e197414c7abe3fd73e3eb8a20b
Source noteuspto-grants-2014_01