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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 436344Generated: October 25, 2026

2-(Trifluoromethyl)aniline → 2-Chloro-6-(trifluoromethyl)aniline

https://huagongshe.com/reaction/436344

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Trifluoromethyl)anilineHCID 6922—
ReactantBenzenamine, 4-chloro-2-(trifluoromethyl)-HCID 67961—
Reactant2,4-Dichloro-6-(trifluoromethyl)anilineHCID 1268255—
Product2-Chloro-6-(trifluoromethyl)anilineHCID 2756384—

Reaction Steps

VPC assay of the organic product revealed the following composition (15% XE 60 column packing; 120° C-250° C; 4°/min.): o-aminobenzotrifluoride (13.1 wt. %; 25.94 grams; 0.161 mole; 83.9% conversion); 2-amino-5-chlorobenzotrifluoride, 53.5 wt. %; 105.9 grams or 64.5% corrected yield); and, 2-amino-3,5-dichlorobenzotrifluoride, 33.3 wt. %; 65.93 grams or 34.2% corrected yield). A trace of 2-amino-3-chlorobenzotrifluoride was produced.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04008278
Source datasetuspto-grants-1977_02
ORD IDord-4ab88bc022c74ed3b3b8242e8e8c522a
Source noteuspto-grants-1977_02