HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 451034Generated: October 30, 2026
Isocyanatocarbonyl chloride → HCID 58075569, compound
https://huagongshe.com/reaction/451034
Participants
| Role | Name | HCID | Charge |
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| Reactant | Isocyanatocarbonyl chloride | HCID 119708 | — |
| Reactant | HCID 24787891 | HCID 24787891 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 58075569 | HCID 58075569 | 52.6% |
Reaction Steps
A mixture of 2-(4-fluorophenyl)cyclopentanone (18.557 g, 104 mmol) and carbonisocyanatidic chloride (19.77 g, 187 mmol) was heated at 58° C. for 1 h and at 130° C. for 2 h. Upon cooling to room temperature, the tarrified reaction mixture 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 with ethyl acetate. The combined organic extracts were dried over anhydrous magnesium sulfate and filtered. The solvent was removed in vacuum and the residue was purified by column chromatography on silica gel to give 7-(4-fluorophenyl)-6,7-dihydrocyclopenta[e][1,3]oxazine-2,4(3H,5H)-dione (13.527 g, 54.7 mmol, 52.5% yield) as brown solid. LC-MS (M+H)+=248.1. 1H NMR (500 MHz, CDCl3) δ ppm 11.80 (1H, br s), 7.31-7.39 (2H, m), 7.16-7.22 (2H, m), 4.30-4.38 (1H, m), 2.63-2.73 (1H, m), 2.53-2.63 (2H, m), 1.84-1.95 (1H, m).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08486952B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-ad147416cc394898a0d07f19880fb64b |
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| Source note | uspto-grants-2013_07 |
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