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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2094790Generated: November 1, 2026

Pyridine → HCID 86648442, compound

https://huagongshe.com/reaction/2094790

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantTrichloroacetyl chlorideHCID 6420—
Reactant4-Chloro-3-(trifluoromethyl)anilineHCID 67574—
SolventDichloromethaneHCID 6344—
ProductHCID 86648442HCID 8664844279.1%

Reaction Steps

The clear solution of 3-trifluoromethyl-4-chloroaniline (45 g, 0.230 mol) and pyridine (37 ml, 0.460 mol) in dichloromethane (450 ml) cooled at 0° C. to −5° C. and a solution of trichloroacetyl chloride (31 ml, 0.2876 mol) in dichloromethane (100 ml) was added drop wise maintaining temperature of the reaction mass below 0° C. The reaction mass was then stirred for 1 hour below 0° C. and quenched with water (250 ml) below 5° C. The organic phase was separated and aqueous layer was re-extracted with dichloromethane. The combined dichloromethane layer was washed with water, dried over sodium sulfate and evaporated under vacuum to obtain (62 g) of 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-13278e18e6284852b1662eda2fe5f79e
Source noteuspto-grants-2013_05