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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2277690Generated: October 30, 2026

Methanol → Methyl 2-(5-bromopyridin-3-yl)acetate

https://huagongshe.com/reaction/2277690

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantThionyl ChlorideHCID 24386—
Reactant2-(5-Bromopyridin-3-yl)acetic acidHCID 2802539—
ProductMethyl 2-(5-bromopyridin-3-yl)acetateHCID 23398394—

Reaction Steps

To a solution of (5-bromo-pyridin-3-yl)-acetic acid (4.2 g, 20 mmol) in methanol (50 mL) was added thionyl chloride (4.4 mL, 60 mmol) slowly at 0° C. After the addition, the reaction mixture was warmed up and heated to reflux temperature for 2 hours. After cooling back to room temperature, the reaction mixture was concentrated in vacuo and the residue was re-dissolved in EtOAc (250 mL) and washed with aq. NaHCO3 solution and brine. The organic layer was dried over Na2SO4, filtered and concentrated in vacuo to give a crude product (4.6 g, quant.) as light yellow solid. MS: 230.1 & 232.0 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09133158B2
Source datasetuspto-grants-2015_09
ORD IDord-6483e90d551a4697844594f01a0e0eb9
Source noteuspto-grants-2015_09