HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → 1-(Chloromethyl)-4-(methylthio)benzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | [4-(Methylsulfanyl)phenyl]methanol | HCID 592968 | — |
| Catalyst | Pyridine | HCID 1049 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 1-(Chloromethyl)-4-(methylthio)benzene | HCID 70128 | 90.1% |
Reaction Steps
To a solution of 50.0 g (325 mMol) of 4-(methylthio)benzyl alcohol in 350 ml of toluene stirring at room temperature under nitrogen, was added 5 drops of pyridine, and then 28.4 ml (46.4 g, 390 mMol, 1.2 eqs) of thionyl chloride was added dropwise. After 3 hours, ice water was added and the mixture was stirred for 20 minutes. The mixture was transferred to a separatory funnel and shaken thoroughly. The organic layer separated and was dried over sodium sulfate, filtered, and evaporated. Distillation of the residue under reduced pressure gave (4-methylthiophenyl)chloromethane (50.54 g) as a colorless liquid: b.p. 89°-95° C. (1 mm).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05686470 |
| Source dataset | uspto-grants-1997_11 |
| ORD ID | ord-4124232dbf724f5cb494cee99a4f642c |
| Source note | uspto-grants-1997_11 |