HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 255875Generated: October 31, 2026
Thionyl Chloride → HCID 20165021, compound
https://huagongshe.com/reaction/255875
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 2-[[3-(Trifluoromethyl)phenyl]amino]ethanol | HCID 15636103 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 20165021 | HCID 20165021 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04699910 |
|---|
| Source dataset | uspto-grants-1987_10 |
|---|
| ORD ID | ord-c6031db4fb004af8881e87e11833fbef |
|---|
| Source note | uspto-grants-1987_10 |
|---|