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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 394884생성일: 2026년 10월 24일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물FormamideHCID 713—
반응물Sodium HydroxideHCID 14798—
반응물Phosphorus sulfide (P2S5)HCID 14817—
반응물MethanethioamideHCID 3005587—
반응물2-Bromo-1-(4-hydroxy-2-methylphenyl)ethanoneHCID 17812170—
용매1,4-DioxaneHCID 31275—
생성물3-Methyl4-(1,3-thiazol-4-yl)phenolHCID 2231380877%

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06603008B1
출처 데이터셋uspto-grants-2003_08
ORD IDord-e2395ef115234865b5f005966c1aa5c8
출처 메모uspto-grants-2003_08