HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbon Tetrachloride → 2,4-Difluorobenzoyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbon Tetrachloride | HCID 5943 | — |
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 2,4-Difluorobenzoic acid, 2-phenylhydrazide | HCID 15117048 | — |
| Product | 2,4-Difluorobenzoyl chloride | HCID 588081 | 89% |
Reaction Steps
To a stirred mixture, under nitrogen, of 49.6 g of 2,4-difluorobenzoic acid, 2-phenylhydrazide, 64.3 g of triphenylphosphine, and 500 ml of anhydrous acetonitrile was added 19.3 ml of carbon tetrachloride. The reaction mixture was stirred at ambient temperature for about 16 hours, concentrated, and extracted with diethyl ether (3×). The diethyl ether extract was filtered and concentrated to a residue, which was flash chromatographed on silica gel, eluting first with ethyl acetate-hexane and, in a subsequent run, with ethyl acetate alone. Concentration of the appropriate fractions yielded 47.5 g (89%) of α-chloro-2,4-difluorobenzaldehyde, phenylhydrazone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05134236 |
| Source dataset | uspto-grants-1992_07 |
| ORD ID | ord-d2a0cb4d314d4a8194e28b70fb0d817a |
| Source note | uspto-grants-1992_07 |