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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1721605Generated: November 2, 2026

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

https://huagongshe.com/reaction/1721605

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 numberUS05512561
Source datasetuspto-grants-1996_04
ORD IDord-4b421fd078a84a14bab0d2da0427d926
Source noteuspto-grants-1996_04