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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 554711Generated: October 31, 2026

4-Chloroaniline → HCID 3092418, compound

https://huagongshe.com/reaction/554711

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-ChloroanilineHCID 7812—
ReactantPhosphorus pentachlorideHCID 24819—
ReactantHCID 3090003HCID 3090003—
Reactant4-Bromo-N-(1,2,2,2-tetrachloroethyl)benzamideHCID 59192635—
SolventChloroformHCID 6212—
ProductHCID 3092418HCID 3092418—

Reaction Conditions

Temperature50 °C

Reaction Steps

A solution of 4-bromo-N-(2,2,2-trichloro-1-hydroxyethyl)benzamide (0.67 g, 1.93 mmol) in chloroform (15 mL) was treated with PCl5 (0.42 g, 1.91 mmol). The mixture was heated to 50° C. for 30 minutes before cooling to room temperature and pouring into crushed ice. The organic layer was dried over MgSO4 and filtered. The solution of 4-bromo-N-(1,2,2,2-tetrachloroethyl)benzamide was cooled to room temperature before addition of 4-chloroaniline (0.52 mL, 4.0 mmol), and the mixture was allowed to stir for 18 hours. The mixture was quenched with 2 M HCl and extracted with ether. The organic solution was dried over MgSO4, filtered, and concentrated onto silica gel. The material was purified on an MPLC with 7:3 CH2Cl2:hexanes to give 4-bromo-N-(2,2,2-trichloro-1-(4-chlorophenylamino)ethyl)benzamide (Compound 6) as a solid. The product may be further purified by an appropriate recrystallization such as in ether.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08049037B2
Source datasetuspto-grants-2011_11
ORD IDord-53b914c76ffd408b92c4bd9d22d53f92
Source noteuspto-grants-2011_11