HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1649326Generated: October 31, 2026
Ethyl trichloroacetate → HCID 12292572, compound
https://huagongshe.com/reaction/1649326
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl trichloroacetate | HCID 10588 | — |
| Reactant | 2-Oxazolidinone | HCID 73949 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Product | HCID 12292572 | HCID 12292572 | 89% |
Reaction Steps
A mixture of 2-oxazolidinone (9.0 g, 0.10 mole) and 25 ml (0.18 mole) of ethyl trichloroacetate were heated to 120° C. in an oil bath. A small amount (ca 50 mg) of 4-dimethylaminopyridine was added to the stirred solution, during which time vigorous reflux began. After removing most of the chloroform by a Dean-Stark trap, the dark solution was allowed to cool to room temperature. Bulb to bulb distillation at 105° C.-120° C. (0.05 mm) yielded 14.1 g (0.0887 mole, 89 percent yield) of the product as a clear liquid which solidified to a colorless solid (mp 40° C.-44° C.) on standing at room temperature. Spectral data confirmed its structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04416818 |
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| Source dataset | uspto-grants-1983_11 |
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| ORD ID | ord-7dcfdac66ef640cf8b58e28e5cb95e79 |
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| Source note | uspto-grants-1983_11 |
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