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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2362359Generated: November 1, 2026

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

https://huagongshe.com/reaction/2362359

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantThionyl ChlorideHCID 24386—
Reactant2-(5-Bromopyridin-3-yl)acetic acidHCID 2802539—
SolventMethanolHCID 887—
ProductMethyl 2-(5-bromopyridin-3-yl)acetateHCID 2339839489%

Reaction Steps

2-(5-bromopyridin-3-yl)acetic acid (5.00 g, 23.14 mmol) in methanol (55 mL) at 0° C. was added thionyl chloride (2.196 mL, 30.1 mmol) slowly, pyridine (2.434 mL, 30.1 mmol) was added slowly after and the reaction was stirred at room temperature overnight. Solvent was removed in vacuo and the residue was diluted with water and extracted with ethyl acetate, the organics was washed with brine, dried over magnesium sulfate, filtered and concentrated. Biotage purification (35% EtOAc/Hex) gave title compound (4.73 g, 20.6 mmol, 89% yield). 1H-NMR (CDCl3, 500 MHz) δ 8.63 (d, J=2.14 Hz, 1H), 8.47 (d, J=1.83 Hz, 1H), 7.84 (dd, J=2.14, 1.83 Hz, 1H), 3.76 (s, 3H), 3.65 (s, 2H). Mass spec.: 230.9 (MH)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08691821B2
Source datasetuspto-grants-2014_04
ORD IDord-425356a58ccb4e6d9ddc7da31850e806
Source noteuspto-grants-2014_04