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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1525844Generated: November 2, 2026

4-Bromophenacyl bromide → HCID 1130426, compound

https://huagongshe.com/reaction/1525844

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Bromophenacyl bromideHCID 7454—
ReactantProthionamideHCID 666418—
SolventEthanolHCID 702—
ProductHCID 1130426HCID 113042679.6%

Reaction Conditions

Temperature70 °C

Reaction Steps

As shown in FIG. 27, in reaction (a) a mixture of prothionamide (9.01 g, 50.0 mmol) and 4-bromophenacyl bromide 6a (13.9 g, 50.0 mmol) in EtOH (400 mL) was stirred at 70° C. for 1 h. After cooled to room temperature, the precipitation was filtered off with EtOAc and washed with EtOAc and saturated aqueous NaHCO3. The organic layer was washed with brine, dried over Na2SO4, and concentrated to give 4-(4-bromophenyl)-2-(2-propylpyridin-4-yl)thiazole 2 (14.3 g, 79%) as a light-yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09085566B2
Source datasetuspto-grants-2015_07
ORD IDord-29c6c30d054c46bcbbe12d3c87577621
Source noteuspto-grants-2015_07