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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1499118Generated: November 2, 2026

Oxalyl chloride → Methyl 2-chloro-6-methylpyridine-3-carboxylate

https://huagongshe.com/reaction/1499118

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
Reactant2-Chloro-6-methylnicotinic acidHCID 121724—
SolventDichloromethaneHCID 6344—
ProductMethyl 2-chloro-6-methylpyridine-3-carboxylateHCID 13055804—

Reaction Steps

To the solution of 2-chloro-6-methylnicotinic acid (5 g, 29.1 mmol) in CH2Cl2 (40 mL) was added oxalyl dichloride (8.1 g, 63.8 mmol) at 0° C. and the reaction mixture was stirred for 2 h. The mixture was concentrated and 40 mL of methanol was then added at 0° C. and the reaction mixture was stirred at RT for 12 h. The mixture was then concentrated in vacuo and extracted with EtOAc. The combined organic layers were washed with brine, dried over Na2SO4, filtered, and concentrated in vacuo to provide methyl 2-chloro-6-methylnicotinate that is used without further purification as a light yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09199994B2
Source datasetuspto-grants-2015_12
ORD IDord-568c4cce789a46f984593b2ddc98f41a
Source noteuspto-grants-2015_12