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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2234222Generated: November 1, 2026

Thionyl Chloride → 2-Chloro-5-(chloromethyl)-3-methoxypyridine

https://huagongshe.com/reaction/2234222

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant(6-Chloro-5-methoxypyridin-3-yl)methanolHCID 59297074—
SolventDichloromethaneHCID 6344—
Product2-Chloro-5-(chloromethyl)-3-methoxypyridineHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07709649B2
Source datasetuspto-grants-2010_05
ORD IDord-188665bf791d4779bc8545ca2bd1f113
Source noteuspto-grants-2010_05