HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → 4-(4-Trifluoromethylbenzyloxy)-2-chloromethylpyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 4-(4-Trifluoromethylbenzyloxy)-2-hydroxymethylpyridine | HCID 14425972 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-(4-Trifluoromethylbenzyloxy)-2-chloromethylpyridine | HCID 14425986 | — |
Reaction Steps
2.2 g (7.8 mmol) of the title compound from Example 3 are dissolved in 50 ml of anhydrous dichloromethane and a solution of 2 ml of thionyl chloride in 6 ml of dichloromethane is added dropwise at -10° C. The mixture is warmed to room temperature, stirred for 30 minutes more, and concentrated. The crystalline residue is brought to crystallization using diisopropyl ether and dried using an oilpump, m.p. 133°-135° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05114955 |
| Source dataset | uspto-grants-1992_05 |
| ORD ID | ord-a9a3fc14b80044d4ada986a19f0862a4 |
| Source note | uspto-grants-1992_05 |