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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2370155Generated: October 30, 2026

Isocyanatocarbonyl chloride → HCID 58075794, compound

https://huagongshe.com/reaction/2370155

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsocyanatocarbonyl chlorideHCID 119708—
Reactant2-(4-Chlorophenyl)cyclopentan-1-oneHCID 13023806—
SolventEthyl AcetateHCID 8857—
ProductHCID 58075794HCID 5807579451.1%

Reaction Conditions

Temperature130 °C

Reaction Steps

A solution of 2-(4-chlorophenyl)cyclopentanone (7.80 g, 40.1 mmol) and carbonisocyanatidic chloride (7.61 g, 72.1 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-(4-chlorophenyl)-6,7-dihydrocyclopenta[e][1,3]oxazine-2,4(3H,5H)-dione (5.4 g, 20.48 mmol, 51.1% yield). LC-MS (M+H)+=264.2. 1H NMR (500 MHz, CDCl3) δ ppm 7.32 (2H, d, J=8.5 Hz), 7.12 (2H, d, J=8.5 Hz), 4.15-4.25 (1H, m), 2.56-2.93 (4H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08710061B2
Source datasetuspto-grants-2014_04
ORD IDord-5df52bad4b554acbbf693ccb22d0628c
Source noteuspto-grants-2014_04