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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 37359Generated: October 29, 2026

Toluene → 2-Bromo-5-(chloromethyl)pyridine

https://huagongshe.com/reaction/37359

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantSodium HydroxideHCID 14798—
ReactantThionyl ChlorideHCID 24386—
Reactant6-Bromo-3-pyridinemethanolHCID 6421249—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
Product2-Bromo-5-(chloromethyl)pyridineHCID 6424658134%

Reaction Steps

To a mechanically-stirred solution of 78.12 g of thionyl chloride in 450 mL of acetonitrile at 15° C. was added a solution of 160.75 g of 3-hydroxymethyl-6-bromopyridine in 446 mL of acetonitrile over 30 minutes. The temperature rose to 22° C. during the addition, and the reaction mixture was stirred for 15 minutes at room temperature. The mixture was cooled in an ice bath, and a solution of 70 g of NaOH in 1.4 L of water was added at such a rate that the temperature did not exceed 15° C. 603 mL of toluene was added to the mixture and stirred rapidly. The layers were separated. The aqueous phase was reextracted with toluene. The combined organic phase was concentrated in vacuo to give 181.61 g of 3-chloromethyl-6-bromopyridine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05420270
Source datasetuspto-grants-1995_05
ORD IDord-9a8cc4f9960f4607baafb2e96f52d3be
Source noteuspto-grants-1995_05