HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → 3-Fluoro-4-(trifluoromethyl)benzyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 3-Fluoro-4-(trifluoromethyl)benzyl alcohol | HCID 2737562 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 3-Fluoro-4-(trifluoromethyl)benzyl chloride | HCID 22262070 | 87% |
Reaction Steps
To absolution of 3-fluoro-4-(trifluoromethyl)benzyl alcohol (10 g, 52 mmol) in chloroform (20 ml) was added thionyl chloride (18.5 ml, 257 mmol) and the mixture was heated under ref lux for 4 hrs. The reaction solution was concentrated. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=4:1) to give 3-fluoro-4-(trifluoromethyl)benzyl chloride (9.52 g, 87%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06982348B2 |
| Source dataset | uspto-grants-2006_01 |
| ORD ID | ord-bb96693162034c8f9ed3547559716fc4 |
| Source note | uspto-grants-2006_01 |