HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → 2-Chloro-5-(chloromethyl)-3-methoxypyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | (6-Chloro-5-methoxypyridin-3-yl)methanol | HCID 59297074 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Chloro-5-(chloromethyl)-3-methoxypyridine | HCID 59297073 | — |
Reaction Steps
To a solution of (6-chloro-5-methoxypyridin-3-yl)methanol (0.50 g, 2.9 mmol) in dichloromethane (14 mL) at 25° C. was added thionyl chloride (230 μL, 3.2 mmol) dropwise. Let stir for 5 h, then the reaction was quenched with saturated aqueous NaHCO3 and extracted with dichloromethane (3×). The combined organic layer were dried over MgSO4 and concentrated to furnish the product 2-chloro-5-chloromethyl-3-methoxypyridine that was 96% pure by GC-MS. The product was used immediately in the next step without further purification. GC-MS: Exact mass calcd for C7H7Cl2NO [M]+, 191. Found 191.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07709649B2 |
| Source dataset | uspto-grants-2010_05 |
| ORD ID | ord-188665bf791d4779bc8545ca2bd1f113 |
| Source note | uspto-grants-2010_05 |