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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 633712Generated: October 30, 2026

4-Methyl-5-(2-hydroxyethyl)thiazole → 5-(2-bromoethyl)-4-methylthiazole

https://huagongshe.com/reaction/633712

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Methyl-5-(2-hydroxyethyl)thiazoleHCID 1136—
ReactantTriphenylphosphineHCID 11776—
ReactantN-bromobutanimideHCID 67184—
SolventDichloromethaneHCID 6344—
Product5-(2-bromoethyl)-4-methylthiazoleHCID 20418762.6%

Reaction Conditions

Temperature0 °C

Reaction Steps

1 g (6.98 mmol) of 2-(4-methylthiazol-5-yl)ethanol is dissolved in 15 mL of dichloromethane. The solution is cooled to 0° C. When the temperature is reached, 1.85 g (6.98 mmol) of triphenylphosphine are added, followed by portionwise addition of 1.30 g (6.98 mmol) of N-bromosuccinimide. After stirring for 2 hours at 0° C., the mixture is evaporated to dryness. The residue is purified by chromatography on silica gel (eluent: 50/50 EtOAc/heptane) to give 900 mg of 5-(2-bromoethyl)-4-methylthiazole, the characteristics of which are as follows:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09321790B2
Source datasetuspto-grants-2016_04
ORD IDord-d1814a2221f348e489e0a298cd611760
Source noteuspto-grants-2016_04