HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 544259Generated: October 31, 2026
Ethylene carbonate → HCID 13259764, compound
https://huagongshe.com/reaction/544259
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethylene carbonate | HCID 7303 | — |
| Reactant | Acifluorfen | HCID 44073 | — |
| Catalyst | Tetraethylammonium Iodide | HCID 6225 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 13259764 | HCID 13259764 | — |
Reaction Steps
A mixture of 5-(2-chloro-4-trifluoromethylphenoxy)-2-nitrobenzoic acid (7.24 g, 0.02 mole), ethylene carbonate (2.0 g, 0.023 mole) and tetraethylammonium iodide (1.0 g) was heated in an oil bath at 105°-110° C. for 10 hrs. The reaction was completed and the resulting gummy material was taken into 300 ml of ether. The ethereal solution was washed three times with water and dried over CaSO4. After the solvent had been removed, the product was crystallized from toluene/hexane and an almost quantitative yield (>95%) of the desired ester was obtained as a light brown crystalline solid; m.p. 71°-74° C., NMR (CDCl3) 3.33 (S, 1H), 3.67-4.12 (m, 2H), 4.15-4.63 (m, 2H), 7.02-8.25 (m, 6H); ir (CHCl3) 1749 cm-1. No by-product was detected by NMR analysis.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04448982 |
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| Source dataset | uspto-grants-1984_05 |
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| ORD ID | ord-4dcaabe3db6a421f9d9cb9ce800d69f8 |
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| Source note | uspto-grants-1984_05 |
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