HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → 3-(Methylsulfonyl)-5-(trifluoromethyl)benzoyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 71766083 | HCID 71766083 | — |
| Catalyst | Dimethylformamide | HCID 6228 | — |
| Product | 3-(Methylsulfonyl)-5-(trifluoromethyl)benzoyl chloride | HCID 86670808 | 102.9% |
Reaction Steps
To 3-(methylsulfonyl)-5-(trifluoromethyl)benzoic acid (1 g, 3.73 mmol, example 1, intermediate d) was added N,N-dimethylformamide (27.3 mg, 28.9 μL, 373 μmol) and thionyl chloride (8.87 g, 5.44 ml, 74.5 mmol) and the suspension was heated to reflux for 30 min. A light brown solution was formed. To remove thionyl chloride, the light brown solid was diluted with toluene, followed by complete evaporation. This procedure was repeated two times to provide the desired compound as a colorless solid (1.1 g; 99%) which was pure enough for the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08748434B2 |
| Source dataset | uspto-grants-2014_06 |
| ORD ID | ord-14b60bfe2f4b41238fc2159eb0034bb1 |
| Source note | uspto-grants-2014_06 |