HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-(Trifluoromethyl)benzamide → 4-(Trifluoromethyl)thiobenzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-(Trifluoromethyl)benzamide | HCID 74684 | — |
| Reactant | Lawesson's reagent | HCID 87949 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 4-(Trifluoromethyl)thiobenzamide | HCID 2734823 | — |
Reaction Steps
A mixture of 4-trifluoromethylbenzamide (79 mM) and Lawesson's reagent (39 mM) in toluene (200 mL) was heated at reflux for 4 hours under N2. The reaction mixture was cooled and the resulting precipitate was isolated by filtration to give 4-trifluoromethylthiobenzamide as a solid: mp 125° C. (The following general procedure was used to synthesize the various substituted thiobenzamides (Tetrahedron 35,2433, (1979)):
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05342851 |
| Source dataset | uspto-grants-1994_08 |
| ORD ID | ord-492d5f40d4ba43ef87ff13b54b9e01ed |
| Source note | uspto-grants-1994_08 |