Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 255875Generated: October 31, 2026

Thionyl Chloride → HCID 20165021, compound

https://huagongshe.com/reaction/255875

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant2-[[3-(Trifluoromethyl)phenyl]amino]ethanolHCID 15636103—
SolventDichloromethaneHCID 6344—
ProductHCID 20165021HCID 20165021—

Reaction Conditions

Temperature0 °C

Reaction Steps

20.5 g (0.1 mole of N-(2-hydroxy-ethyl)-3-trifluoromethyl-aniline were taken up in 100 ml of absolute methylene chloride, and the solution was cooled to 0° C. At this temperature 14.3 g (0.12 mol) of thionyl chloride were added dropwise. The reaction mixture was allowed to warm to room temperature while stirring, whereupon it was refluxed, while monitoring by chromatography, until the reaction had gone to completion. After the solvent and the residual thionyl chloride had been removed, the crude product thus obtained was used for further reaction.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04699910
Source datasetuspto-grants-1987_10
ORD IDord-c6031db4fb004af8881e87e11833fbef
Source noteuspto-grants-1987_10