HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → 1-(Chlorophenylmethyl)-4-fluorobenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 4-Fluorobenzhydrol | HCID 570753 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-(Chlorophenylmethyl)-4-fluorobenzene | HCID 216256 | 95.2% |
Reaction Steps
In dichloromethane (30 mL), (±)-(4-fluorophenyl)phenylmethanol (2.1 g, 10 mmol) synthesized in Production Example 195 was dissolved, and thionyl chloride (5.1 g, 42 mmol) was added dropwise thereto at a room temperature. After the completion of the dropping, the mixture was heated under reflux, and the completion of the reaction was confirmed by TLC. After the completion of the reaction, the reaction mixture was concentrated, diluted with ethyl acetate, and washed with water. The organic layer was dried over magnesium sulfate, and the solvent was distilled off. Thus the title compound (2.1 g, 94%) was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09365553B2 |
| Source dataset | uspto-grants-2016_06 |
| ORD ID | ord-5873cc4dd1494309bcc9ab90319b79c8 |
| Source note | uspto-grants-2016_06 |