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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2094774Generated: October 31, 2026

Pyridine → HCID 86648442, compound

https://huagongshe.com/reaction/2094774

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantTrichloroacetyl chlorideHCID 6420—
Reactant4-Chloro-3-(trifluoromethyl)anilineHCID 67574—
SolventDichloromethaneHCID 6344—
ProductHCID 86648442HCID 8664844290.2%

Reaction Steps

The clear solution of 3-trifluoromethyl-4-chloroaniline (35 g, 0.1789 mol) and pyridine (36 ml, 0.447 mol) in dichloromethane (350 ml) was cooled at 0° C. to −5° C. and a solution of trichloro acetyl chloride (26 ml, 0.2326 mol) in dichloromethane (75 ml) was added drop wise maintaining temperature of the reaction mass below 0° C. The reaction mass was stirred for 1 hour below 0° C. and quenched with water (150 ml) below 5° C. The organic phase was separated and aqueous layer was reextracted with dichloromethane. The combined dichloromethane layer was then washed with water, dried over sodium sulfate and evaporated under vacuum to obtain (55 g) the desired product, i.e., 2,2,2-trichloro-N-(4-chloro-3-(trifluoromethyl)phenyl)acetamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08445687B2
Source datasetuspto-grants-2013_05
ORD IDord-617b6e10f0b14584b71669133678e6ab
Source noteuspto-grants-2013_05