HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → 2,5-Difluoro-4-Methylbenzoyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 2,5-Difluoro-4-methylbenzoic acid | HCID 13657451 | — |
| Product | 2,5-Difluoro-4-Methylbenzoyl chloride | HCID 13657457 | — |
Reaction Steps
250 ml of thionyl chloride are taken and 120 g of 2,5-difluoro-4-methyl-benzoic acid are introduced in portions at room temperature, with brisk evolution of gas. When the evolution of gas has subsided, the mixture is heated slowly to the reflux temperature and stirred until the evolution of gas has ended. The excess thionyl chloride is distilled off, the reaction product is coarsely distilled over and the distillate is fractionated on a small column. Yield: 97 g (72.9% of theory) of 2,5-difluoro-4-methylbenzoyl chloride of boiling point b.p.: 103°/20 mbar, nD20 : 1.5232.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04762844 |
| Source dataset | uspto-grants-1988_08 |
| ORD ID | ord-8f63d8c795b44489840f46bc733e1d03 |
| Source note | uspto-grants-1988_08 |