HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → 4-(Methylthio)-3-(trifluoromethyl)benzyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 68663620 | HCID 68663620 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 4-(Methylthio)-3-(trifluoromethyl)benzyl chloride | HCID 68663128 | 78.2% |
Reaction Steps
To a solution of 4-(methylthio)-3-(trifluoromethyl)benzyl alcohol (3.00 g, 13.5 mmol) in toluene (15 mL) was added thionyl chloride (1.18 mL, 16.2 mmol) at room temperature, and the resulting mixture was stirred for 1 hr. The reaction mixture was concentrated under reduced pressure. The residue was purified by basic silica gel column chromatography (hexane/ethyl acetate=10/1), and crystallized from hexane to give the title compound (2.54 g, yield 78%) as colorless crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08492378B2 |
| Source dataset | uspto-grants-2013_07 |
| ORD ID | ord-fbc4c5979b714003bab4103f73dc3040 |
| Source note | uspto-grants-2013_07 |