HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → 2-(Benzyloxy)-6-(chloromethyl)pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | (6-(Benzyloxy)pyridin-2-yl)methanol | HCID 21193214 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 2-(Benzyloxy)-6-(chloromethyl)pyridine | HCID 21193174 | — |
Reaction Steps
A mixture of 2-benzyloxy-6-hydroxymethylpyridine (1.5 g, 7.0 mmol) and thionyl chloride (10 mL, 137 mmol) in benzene (25 mL) was stirred at room temp. overnight. The product mixture was concentrated under vacuum. The residue was partitioned between chloroform and aqueous sodium bicarbonate. The organic extract was washed with brine, dried over anhydrous sodium sulfate, filtered and concentrated under vacuum. The residue was subjected to column chromatography on silica gel eluting with 5% methanol in chloroform. Collection and concentration of appropriate fractions provided 2-benzyloxy-6-chloromethylpyridine as clear, colorless 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-b1199d2dc1974ab89c405153a163004d |
| Source note | uspto-grants-1999_04 |