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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 271472Generated: October 25, 2026

Ethyl Acetate → 5-Chloro-2-(chloromethyl)pyridine

https://huagongshe.com/reaction/271472

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantSodium CarbonateHCID 10340—
ReactantThionyl ChlorideHCID 24386—
Reactant(5-Chloropyridin-2-yl)methanolHCID 20537893—
CatalystDimethylformamideHCID 6228—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product5-Chloro-2-(chloromethyl)pyridineHCID 1451715189.4%

Reaction Steps

To a stirring solution of (5-chloropyridin-2-yl)methanol (840 mg, 5.8 mmol) in dichloromethane (10 mL) at 0° C. under argon was added thionyl chloride (0.64 mL, 8.77 mmol), followed by 4 drops of DMF (white precipitate formed). The reaction mixture was allowed to stir at room temperature for 1 h. The reaction mixture was concentrated to a white solid. The solid thus obtained was cooled in an ice bath before EtOAc (20 mL) and water (20 mL) and then 10% aqueous Na2CO3 solution (20 mL) were added. The organic layer was separated, washed with saturated aqueous NaCl, dried (MgSO4), filtered and concentrated to obtain 840 mg of the title compound as a light brown gum. HPLC/MS: retention time=2.392 min, [M+H]+=162.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07452892B2
Source datasetuspto-grants-2008_11
ORD IDord-9f8450a03e8f493db052c87b82442419
Source noteuspto-grants-2008_11