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HRID 394884作成日:2026年10月24日

Formamide → 3-Methyl4-(1,3-thiazol-4-yl)phenol

https://huagongshe.com/ja/reaction/394884

反応式

関与物質

役割名称HCID仕込み量
反応物FormamideHCID 713—
反応物Sodium HydroxideHCID 14798—
反応物Phosphorus sulfide (P2S5)HCID 14817—
反応物MethanethioamideHCID 3005587—
反応物2-Bromo-1-(4-hydroxy-2-methylphenyl)ethanoneHCID 17812170—
溶媒1,4-DioxaneHCID 31275—
生成物3-Methyl4-(1,3-thiazol-4-yl)phenolHCID 2231380877%

反応手順

To a stirred solution of phosphorus pentasulfide (6.0 g, 13.5 mmol) in dioxane (60 ml) was added formamide (7.2 g, 160 mmol), and the mixture was heated at reflux temperature for 2 hours. The reaction mixture was cooled down to room temperature, and the solution was decanted away from solids. To a stirred solution of 2-bromo-1-(4-hydroxy-2-methylphenyl)-1-ethanone from step 1 (2.4 g, 10.5 mmol) in dioxane (20 ml) was added the thioformamide solution, and the mixture was heated at reflux temperature for 6 hours. The reaction mixture was cooled down to room temperature, and made basic by addition of 0.5M NaOH aqueous solution. The whole was extracted with ethyl acetate. The organic layer was washed with brine, dried over MgSO4, and concentrated in vacuo. The residue was purified by flash chromatography eluting with ethyl acetate-hexane (1:4) to give title compound (1.54 g, 77% yield).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06603008B1
出典データセットuspto-grants-2003_08
ORD IDord-e2395ef115234865b5f005966c1aa5c8
出典メモuspto-grants-2003_08