HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2166797Generated: October 31, 2026
Hydrochloric Acid → 1,2,3-Trichloro-5-(trifluoromethyl)benzene
https://huagongshe.com/reaction/2166797
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 4-Amino-3,5-dichlorobenzotrifluoride | HCID 141094 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1,2,3-Trichloro-5-(trifluoromethyl)benzene | HCID 2733399 | — |
Reaction Steps
2,6-Dichloro-4-trifluoromethylaniline (3.3 kg, prepared as in Example 15) in concentrated hydrochloric acid (25 liters) was stirred for 1 hour and then cooled to -6° C. A solution of sodium nitrite (1.41 kg) in water (3 liters) was added over a period of 4 hours keeping the temperature between -5° and -12°. The mixture was then stirred between -5° and 0° until all solid had dissolved (3.5 hours). The mixture was then added in 2 liter portions over a period of 35 minutes to a solution of cuprous chloride (1.5 kg) in concentrated hydrochloric acid with stirring. The dark solution was left to stand for 30 minutes, filtered, and extracted with dichloromethane (1×15 liters, then 2×10 liters). The extracts were washed with water (2×25 liters) dried (MgSO4) and evaporated under reduced pressure to give 3,4,5-trichlorobenzotrifluoride (2.2 kg) with a boiling range of 98°-100°/40 Torr.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04388472 |
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| Source dataset | uspto-grants-1983_06 |
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| ORD ID | ord-3bfdc07fc1fd490da557c6968c823aa4 |
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| Source note | uspto-grants-1983_06 |
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