HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 342973Generated: October 30, 2026
Ethyl chloroformate → Ethyl 2,6-dichloro-4-(trifluoromethyl)benzoate
https://huagongshe.com/reaction/342973
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 4-Bromo-3,5-dichlorobenzotrifluoride | HCID 1268256 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Ethyl 2,6-dichloro-4-(trifluoromethyl)benzoate | HCID 54315306 | 77.7% |
Reaction Steps
n-Butyllithium (1.6M in hexane, 330 ml) was added dropwise with stirring to a solution of 2,6-dichloro-4-trifluoromethylbromobenzene (163.3 g) in ether while maintaining the temperature below -70° C. The mixture was stirred for 1 hour at -78° C. then ethyl chloroformate (61.7 g) was added while maintaining the temperature below -70° C. The mixture was stirred at room temperature overnight. It was cooled to 0° C. and a saturated aqueous solution of ammonium chloride was added. The layers were separated and the organic layer was washed with water, dried (Na2SO4) and filtered. The filtrate was evaporated to dryness and the residue was distilled to give ethyl 2,6-dichloro-4-trifluoromethylbenzoate (123.9 g) as a colourless liquid bp 90°-96° C. at 5 mmHg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05859283 |
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| Source dataset | uspto-grants-1999_01 |
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| ORD ID | ord-9c5d8526cc0a4f11a0633be9eab03f6d |
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| Source note | uspto-grants-1999_01 |
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