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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1988781Generated: November 4, 2026

Oxalyl chloride → Methyl 3-(3-pyridinyl)benzoate

https://huagongshe.com/reaction/1988781

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
Reactant3-(Pyridin-3-yl)benzoic acidHCID 2795575—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
ProductMethyl 3-(3-pyridinyl)benzoateHCID 413318899%

Reaction Steps

To a suspension of 3-(pyridin-3-yl)benzoic acid (0.8 g, 4 mmol) and N,N-dimethylformide (2 drops) in anhydrous methylene chloride (30 mL) was added oxalyl chloride (0.42 mL, 4.8 mmol) dropwise at 0° C. under argon. The mixture was stirred at RT for 3.5 hr and then concentrated. The yellow solid obtained was dissolved in anhydrous methanol (20 mL) at 0° C. After stirring at RT for 30 min, the mixture was concentrated. The residue was dissolved in ethyl acetate, washed with saturated aqueous sodium bicarbonate solution, brine, and dried over anhydrous sodium sulfate. Concentration gave 0.84 g (99% yield) of methyl 3-(pyridin-3-yl)benzoate as a yellow solid. (M+H)+=214.16.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07642273B2
Source datasetuspto-grants-2010_01
ORD IDord-d716a460a6394892bad9daff7dd7d7da
Source noteuspto-grants-2010_01