戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 415632作成日:2026年10月26日

Bromomethyl 4-methoxyphenyl ketone → 4-(4-Methoxy-phenyl)-2-methyl-thiazole

https://huagongshe.com/reaction/415632

反応式

関与物質

役割名称HCID仕込み量
反応物Bromomethyl 4-methoxyphenyl ketoneHCID 4965—
反応物ThioacetamideHCID 2723949—
溶媒WaterHCID 962—
生成物4-(4-Methoxy-phenyl)-2-methyl-thiazoleHCID 76876569.6%

反応条件

温度140 °C

反応手順

The mixture of thioacetamide (16.0 g, 213 mmol) and 2-bromo-1-(4-methoxy-phenyl)-ethanone (4.0 g, 17.5 mmol) was heated at 140° C. for 24 h under nitrogen atmosphere. After the completion of the reaction mixture (TLC monitoring), water (100 mL) was added and extracted with ethyl acetate (3×100 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, 1% EtOAc-Hexane) to get the desired product (2.5 g, 69%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08088791B2
出典データセットuspto-grants-2012_01
ORD IDord-c9e32ea95042451795a1310255c2ac23
出典メモuspto-grants-2012_01