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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 538621Generated: October 28, 2026

Bromomethyl 3-methoxyphenyl ketone → 4-(3-Methoxyphenyl)-2-methyl-1,3-thiazole

https://huagongshe.com/reaction/538621

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromomethyl 3-methoxyphenyl ketoneHCID 101294—
ReactantThioacetamideHCID 2723949—
SolventWaterHCID 962—
Product4-(3-Methoxyphenyl)-2-methyl-1,3-thiazoleHCID 1924028383%

Reaction Conditions

Temperature140 °C

Reaction Steps

A mixture of thioacetamide (8.0 g, 106.0 mmol) and 2-bromo-1-(3-methoxy-phenyl)-ethanone (2.0 g, 8.81 mmol) was heated at 140° C. for 6 h under nitrogen atmosphere. After completion of the reaction mixture (TLC monitoring), water (50 mL) was added and extracted with ethyl acetate (3×50 mL). The combined organics was washed with water, brine, dried (Na2SO4), filtered and concentrated. The crude residue was purified over silica gel (230-400 M, 2% EtOAc-Hexane) to get the desired product (1.5 g, 83%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08865736B2
Source datasetuspto-grants-2014_10
ORD IDord-f7cdb90aa4ed494686cb82b2e3a88876
Source noteuspto-grants-2014_10