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HRID 6971作成日:2026年10月24日

Methyl p-toluenesulfonate → 3-Methoxy-4,4,4-trifluoro-2-butenoic acid ethyl ester

https://huagongshe.com/ja/reaction/6971

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl p-toluenesulfonateHCID 6645—
反応物Cesium carbonateHCID 10796—
反応物Ethyl 4,4,4-trifluoroacetoacetateHCID 67793—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物3-Methoxy-4,4,4-trifluoro-2-butenoic acid ethyl esterHCID 275886756%

反応条件

温度70 °C

反応手順

To a solution of ethyl 4,4,4-trifluoroacetoacetate (12 mL, 82 mmol) in DMF (80 mL) is added cesium carbonate (26.4 g, 82 mmol). The reaction mixture is heated to 70° C. A solution of methyl p-toluenesulfonate (13.5 mL, 90 mmol) in DMF (30 mL) is then added dropwise during 30 min and the reaction mixture is stirred for an additional 1 hr. After cooling to room temperature, the reaction mixture is diluted with H2O (150 mL) and extracted with Et2O (2×150 mL). The organic extracts are combined and washed with H2O and brine, then dried (Na2SO4), filtered and concentrated to afford the title compound (9.0 g, 56%) as an oil which is used without further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07084170B2
出典データセットuspto-grants-2006_08
ORD IDord-d146ffc4743f46cfb9a96289a70a2846
出典メモuspto-grants-2006_08