HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → 4-(4-Trifluoromethylphenyl)benzylchloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | (4'-(Trifluoromethyl)-[1,1'-biphenyl]-4-yl)methanol | HCID 22015014 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 4-(4-Trifluoromethylphenyl)benzylchloride | HCID 11459921 | 98% |
Reaction Steps
2.89 ml (39.65 mmol) of thionyl chloride dissolved in 10 ml of chloroform are added to a solution of 5.0 g (19.82 mmol) of (4′-trifluoromethylbiphenyl-4-yl)methanol in 40 ml of chloroform, and the mixture is stirred at room temperature for 12 hours. After reaction is complete, the reaction mixture is evaporated to dryness, and the residue is taken up in ethyl acetate and washed with saturated sodium carbonate solution. The organic phase is separated off, dried over sodium sulphate and evaporated after filtration. The resulting crude product is purified by flash chromatography on silica gel (mobile phase: cyclohexane/ethyl acetate 9:1). 5.26 g (19.43 mmol, 98% yield) of a colourless solid are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08609727B2 |
| Source dataset | uspto-grants-2013_12 |
| ORD ID | ord-094c11a69d28425baccba49efd3ec264 |
| Source note | uspto-grants-2013_12 |