HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → 4,4-Difluorocyclohexane-1-carbonyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 4,4-Difluorocyclohexanecarboxylic acid | HCID 2779136 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 4,4-Difluorocyclohexane-1-carbonyl chloride | HCID 18758310 | — |
Reaction Steps
4,4-Difluorocyclohexanecarboxylic acid (118.2 g, 0.72 mol) was dissolved in toluene (296 ml). To the clear solution was added thionyl chloride (261 ml, 3.6 mol) and the resultant solution was heated under reflux for 1.5 hours. A sample was taken and concentrated and 1H-NMR indicated complete conversion to the title compound. The reaction was cooled to room temperature and the thionyl chloride was removed under reduced pressure and replaced with toluene to give the title compound as a toluene concentrate at a total volume of 591 ml.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06667314B2 |
| Source dataset | uspto-grants-2003_12 |
| ORD ID | ord-ee4a44f2ed594671823d17e7904d833e |
| Source note | uspto-grants-2003_12 |