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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1258551Generated: October 26, 2026

Pyridine → 2-Bromo-4-(bromomethyl)-5-methyl-1,3-thiazole

https://huagongshe.com/reaction/1258551

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantThionyl bromideHCID 68176—
Reactant(2-Bromo-5-methylthiazol-4-yl)methanolHCID 58127549—
SolventDichloromethaneHCID 6344—
Product2-Bromo-4-(bromomethyl)-5-methyl-1,3-thiazoleHCID 6719014472%

Reaction Steps

To a stirred solution thionyl bromide (2.27 g, 10.94 mmol, 1.1 eq.) in 25 ml dry DCM, cooled to 5° C., was added dropwise a solution of (2-bromo-5-methyl-1,3-thiazol-4-yl)methanol (2.07 g, 9.94 mmol, 1 eq.) and pyridine (0.865 g, 10.94 mmol, 1.1 eq.) in 15 ml dry DCM. On complete addition, the cooling bath was removed, the reaction warmed to room temperature and stirred 1.5 hr. 100 ml of water and 100 ml of DCM were added and stirring allowed for 2 mins. The organic layer was separated, dried over MgSO4 and evaporated. The residue was purified by chromatography on silica gel to give 2-bromo-4-(bromomethyl)-5-methyl-1,3-thiazole (1.94 g, 72% yield) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08466176B2
Source datasetuspto-grants-2013_06
ORD IDord-d64e7b78604e415bb14d565c873d8b19
Source noteuspto-grants-2013_06