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HRID 68566作成日:2026年10月24日

Trifluoroacetic anhydride → 1-(4-Bromo-5-methyl-thiophen-2-yl)-3-(3,5-dichloro-phenyl)-4,4,4-trifluoro-but-2-en-1-one

https://huagongshe.com/ja/reaction/68566

反応式

関与物質

役割名称HCID仕込み量
反応物Trifluoroacetic anhydrideHCID 9845—
反応物(4-Bromo-5-methyl-thiophen-2-yl)-3-(3,5-dichloro-phenyl)-4,4,4-trifluoro-3-hydroxy-butan-1-oneHCID 86706646—
溶媒TriethylamineHCID 8471—
生成物1-(4-Bromo-5-methyl-thiophen-2-yl)-3-(3,5-dichloro-phenyl)-4,4,4-trifluoro-but-2-en-1-oneHCID 8670664789.9%

反応手順

Triethylamine (53 ml) and trifluoracetic anhydride (38 ml) are added to a solution of -(4-bromo-5-methyl-thiophen-2-yl)-3-(3,5-dichloro-phenyl)-4,4,4-trifluoro-3-hydroxy-butan-1-one (110 g, 77% purity) at 0° C. After 12 hours at room temperature, the reaction is quenched with water (200 ml) and a saturated aqueous solution of NaHCO3. The aqueous phase is separated and further extracted with two times dichloromethane. The organic phases are combined, washed with water, dried over MgSO4 and concentrated in vacuo to yield 1-(4-bromo-5-methyl-thiophen-2-yl)-3-(3,5-dichloro-phenyl)-4,4,4-trifluoro-but-2-en-1-one (95 g, 71% purity) as a brown oil. The crude product is used without further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08822466B2
出典データセットuspto-grants-2014_09
ORD IDord-0caca6190e26406abd559db9e2830918
出典メモuspto-grants-2014_09