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HRID 1616533作成日:2026年10月27日

Thioacetimidic acid 2-(4-methoxyphenyl)-2-oxoethyl ester hydrobromide → 4-(4-Methoxy-phenyl)-2-methyl-thiazole

https://huagongshe.com/reaction/1616533

反応式

関与物質

役割名称HCID仕込み量
反応物Thioacetimidic acid 2-(4-methoxyphenyl)-2-oxoethyl ester hydrobromideHCID 68489019—
触媒ZincchlorideHCID 3007855—
溶媒MethanolHCID 887—
溶媒Sodium BicarbonateHCID 516892—
生成物4-(4-Methoxy-phenyl)-2-methyl-thiazoleHCID 76876592.4%

反応手順

Heat a mixture of thioacetimidic acid 2-(4-methoxyphenyl)-2-oxoethyl ester hydrobromide (10.0 g, 32.9 mmol) and zinc (II) chloride (4.50 g, 33.0 mmol) in methanol (80 mL) at reflux under nitrogen protection for 6.5 hours. Cool the mixture, slowly dilute with saturated NaHCO3 (300 mL), and extract with methylene chloride (400 mL×2). Dry the combined organic extracts over sodium sulfate and remove the solvent under reduced pressure. Purify the crude product by flash column chromatography on silica gel, eluting with hexanes/ethyl acetate (9:1), to provide 4-(4-methoxyphenyl)-2-methylthiazole (6.24 g, 92%): APCI mass spectrum m/z 206 [C11H11NOS+H]+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08765796B2
出典データセットuspto-grants-2014_07
ORD IDord-a1bcfb00b9c04d91bda42a3dfa499caf
出典メモuspto-grants-2014_07