HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → 5-(chloromethyl)-2-methylpyridine hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | (6-Methylpyridin-3-yl)methanol | HCID 11228788 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-(chloromethyl)-2-methylpyridine hydrochloride | HCID 12214339 | — |
Reaction Steps
To a solution of (6-methylpyridin-3-yl)methanol (1.24 g) in THF (12.4 mL) was added thionyl chloride (1.10 mL) under ice-cooling, and the mixture was stirred overnight at room temperature. The reaction mixture was concentrated under reduced pressure, and the obtained residue was suspended in ethyl acetate. The precipitate was collected by filtration, and washed with ethyl acetate-hexane to give the title compound (1.64 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09315458B2 |
| Source dataset | uspto-grants-2016_04 |
| ORD ID | ord-2f95570a6b704641abd4e40931c3ffec |
| Source note | uspto-grants-2016_04 |