HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → 2-(Chloromethyl)-5-methoxypyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 178493791 | HCID 178493791 | — |
| Product | 2-(Chloromethyl)-5-methoxypyridine | HCID 14517153 | — |
Reaction Steps
To a solution of 2-hydroxy-methyl-5-methoxy-pyridine (0.68 g, 4.9 mmol) in dry DCM was added dropwise excess thionyl chloride (2.0 mL), and the mixture was refluxed for 2 hours. The solvent was removed in vacuo, and the residue was taken up in EtOAc and washed with NaHCO3 (aq), dried (MgSO4, and concentrated in vacuo. The extremely volatile 2-chloromethyl-5-methoxy-pyridine was obtained as a solution in ethyl acetate to give (984.0 mg, 83.5%) yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06194437B1 |
| Source dataset | uspto-grants-2001_02 |
| ORD ID | ord-51e56b89b45d460784ead246e3c0a0e5 |
| Source note | uspto-grants-2001_02 |