HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → 1-(1-Chloroethyl)-2-fluorobenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 2-Fluoro-alpha-methylbenzenemethanol | HCID 123066 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 1-(1-Chloroethyl)-2-fluorobenzene | HCID 13564325 | — |
Reaction Steps
Thionyl chloride (100 ml.) was added to a solution of 1-(2-fluorophenyl)ethanol [described by McCall, J.A.C.S. 74, 4809 (1952)] (105 g.) in dry chloroform (200 ml.). After the vigorous initial reaction had subsided, the solution was heated at reflux on a steam bath for 30 minutes. The excess of thionyl chloride was removed by repeated co-distillation with dry toluene and the residue was diluted with diethyl ether, washed with water (2 × 100 ml.), dried over sodium sulphate, filtered and evaporated to a yellow liquid, which was distilled to give 1-(2-fluorophenyl)ethyl chloride (73.2 g.), b.p. 70°-75° C./20 mm.Hg, as a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04067723 |
| Source dataset | uspto-grants-1978_01 |
| ORD ID | ord-97e5ae75f6dc4ff9b4ec9afd062596c0 |
| Source note | uspto-grants-1978_01 |