HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2164512Generated: October 30, 2026
Hydrochloric Acid → 2,3,6-Trichloro-4-(trifluoromethyl)aniline
https://huagongshe.com/reaction/2164512
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Chlorine | HCID 24526 | — |
| Reactant | 3-Chloro-4-(trifluoromethyl)aniline | HCID 67962 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2,3,6-Trichloro-4-(trifluoromethyl)aniline | HCID 13127654 | — |
Reaction Steps
A mixture of 3-chloro-4-trifluoromethylaniline [20 g; described in British patent specification No. 459890] and hydrochloric acid (d:1.18; 12 ml) was suspended in water (600 ml). Chlorine gas (from 13 ml of liquid chlorine) was then passed into the stirred suspension with heating at reflux. On completion of the addition of chlorine gas, stirring was continued for a further 15 minutes. After cooling, the solution thus obtained was extracted with dichloromethane (3×250 ml). The combined organic extracts were washed with water, saturated aqueous sodium bicarbonate solution and water, dried over anhydrous sodium sulphate and evaporated. The red oil thus obtained was distilled (bp 143°-147° C./20 mmHg) to give an orange oil which crystallized on standing to give 2,3,6-trichloro-4-trifluoromethylaniline (12.26 g), m.p. 37°-39° C., in the form of an orange solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04505740 |
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| Source dataset | uspto-grants-1985_03 |
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| ORD ID | ord-295959d012e14f488dc4833ddc31081a |
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| Source note | uspto-grants-1985_03 |
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