HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2370155Generated: October 30, 2026
Isocyanatocarbonyl chloride → HCID 58075794, compound
https://huagongshe.com/reaction/2370155
Participants
| Role | Name | HCID | Charge |
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| Reactant | Isocyanatocarbonyl chloride | HCID 119708 | — |
| Reactant | 2-(4-Chlorophenyl)cyclopentan-1-one | HCID 13023806 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 58075794 | HCID 58075794 | 51.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08710061B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-5df52bad4b554acbbf693ccb22d0628c |
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| Source note | uspto-grants-2014_04 |
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