HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1005481Generated: October 29, 2026
Ammonia → 2,3-Dichloro-6-(trifluoromethyl)benzamide
https://huagongshe.com/reaction/1005481
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 2,3-Dichloro-6-(trifluoromethyl)benzoic acid | HCID 11651803 | — |
| Catalyst | Pyridine | HCID 1049 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 2,3-Dichloro-6-(trifluoromethyl)benzamide | HCID 15456983 | — |
Reaction Steps
To a solution of 250 g of 2,3-dichloro-6-trifluoromethylbenzoic acid in 2 liters of benzene was added 5 drops of pyridine and 172 g of thionyl chloride and then the mixture was heated at reflux for 22 hours. After cooling down, the solution was concentrated under reduced pressure, and 2,3-dichloro-6-trifluoromethylbenzyl chloride obtained was added into 1 liter of 28% aqueous ammonia solution, which has been cooled down to 5° C. over 10 minutes with stirring. Then, the solution was further stirred for 1 hour at room temperature. The reaction mixture was extracted with ethyl acetate, and the extract was washed with water and then with saturated saline solution, and was dried over anhydrous magnesium sulfate. The solvent was distilled under reduced pressure, and the crude crystals obtained were washed with n-hexane and then filtered to give 229 g of the title compound(mp. 118-20° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06054605 |
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| Source dataset | uspto-grants-2000_04 |
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| ORD ID | ord-95de71d43eb2490e873cae9b9aeed6fb |
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| Source note | uspto-grants-2000_04 |
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