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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1042340Generated: October 25, 2026

Pyridine → 2-Bromo-4-(1-bromoethyl)-1,3-thiazole

https://huagongshe.com/reaction/1042340

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantThionyl bromideHCID 68176—
Reactant1-(2-Bromothiazol-4-yl)ethan-1-olHCID 66861317—
SolventDichloromethaneHCID 6344—
Product2-Bromo-4-(1-bromoethyl)-1,3-thiazoleHCID 6686074892.3%

Reaction Steps

To a stirred solution thionyl bromide (0.787 g, 3.78 mmol, 1.05 eq.) in 20 ml dry DCM, cooled to 5° C., was added dropwise a solution of 1-(2-bromo-1,3-thiazol-4-yl)ethanol (0.75 g, 3.60 mmol, 1 eq.) and pyridine (0.285 g, 3.60 mmol, 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 of MgSO4 and evaporated to give 2-bromo-4-(1-bromoethyl)-1,3-thiazole (0.9 g, 84% yield) as a yellow viscous oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08557849B2
Source datasetuspto-grants-2013_10
ORD IDord-6ae5e7cedafb4a5d9f9efd7e5a21f2fd
Source noteuspto-grants-2013_10