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HRID 1440124作成日:2026年10月25日

Acetic Acid → 4-(2,4-Difluorophenyl)-1,1,1-trifluoro-4-hydroxy-3-buten-2-one

https://huagongshe.com/reaction/1440124

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物MethanolHCID 887—
反応物Ethyl trifluoroacetateHCID 9794—
反応物2,4-DifluoroacetophenoneHCID 67770—
反応物Sodium MethoxideHCID 10942334—
溶媒Diethyl EtherHCID 3283—
生成物4-(2,4-Difluorophenyl)-1,1,1-trifluoro-4-hydroxy-3-buten-2-oneHCID 6993477897.4%

反応条件

温度25 °C

反応手順

To a solution of 40.0 g (0.256 moles) 2',4'-difluoroacetophenone (commercially available) in 400 mL diethyl ether at 0° C. was added 40 mL (0.405 moles) ethyl trifluoroacetate. At 5° C., 80 mL of a 25% wt. sodium methoxide in methanol (0.37 moles) were added over 15 minutes. The reaction mixture was stirred overnight at 25° C. The mixture was poured over 300 mL ice water and 21.3 mL (0.37 moles) acetic acid were added. The organic layer was washed two times with water, dried over anhydrous MgSO4, and concentrated in vacuo to give 62.85 g (97%) 4-(2,4-difluorophenyl)-1,1,1-trifluoro-4-hydroxy-3-buten-2-one as a yellow oil; 1HNMR (CDCl3) ppm: 6.61 (s,1H), 6.87 (m, 1H)., 6.97 (m, 1H), 7.97 (m, 1H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05496956
出典データセットuspto-grants-1996_03
ORD IDord-ce1c43850534496baa6781f7002c1305
出典メモuspto-grants-1996_03