HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → 2-(Chloromethyl)-4-methylpyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | (4-Methylpyridin-2-yl)methanol | HCID 12325388 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 2-(Chloromethyl)-4-methylpyridine | HCID 12675261 | — |
Reaction Steps
A mixture of 2-hydroxymethyl-4-methylpyridine (5.48 g, 44.5 mmol) and thionyl chloride (60 mL, 822 mmol) in benzene (150 mL) was stirred at room temp. overnight. The product mixture was concentrated under vacuum. The residue was partitioned between dichloromethane and aqueous sodium bicarbonate. The organic extract was washed with brine, dried over anhydrous sodium sulfate, and filtered. The filtrate was concentrated under vacuum to provide the title compound as oil. This alkylating reagent was passed through a small plug of activated basic alumina immediately before use.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05891889 |
| Source dataset | uspto-grants-1999_04 |
| ORD ID | ord-000206fc93154c64a5aedfe76e8d6694 |
| Source note | uspto-grants-1999_04 |