戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 366928作成日:2026年10月25日

Ethyl 2-methyl-4,4,4-trifluoroacetoacetate → Ethyl 3-hydroxy-2-methyl-4,4,4-trifluorobutyrate

https://huagongshe.com/reaction/366928

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl 2-methyl-4,4,4-trifluoroacetoacetateHCID 2737204—
反応物Sodium borohydrideHCID 4311764—
溶媒EthanolHCID 702—
生成物Ethyl 3-hydroxy-2-methyl-4,4,4-trifluorobutyrateHCID 533787—

反応手順

To a solution of ethyl 3-keto-2-methyl-4,4,4-trifluorobutanoate (20.1 g, 0.10 moles) in 250 ml of absolute ethanol, cooled in an ice bath, was added sodium borohydride (1.0 g, 0.25 moles) in portions with stirring. The cooling bath was removed and the reaction stirred at room temperature for 30 minutes. Acetone (5 ml) was added to quench any remaining sodium borohydride and the solvents removed by distillation at atmospheric pressure using a Vigreaux column. The residue was diluted with 200 ml of methylene chloride and poured into a separatory funnel containing 75 ml of a 1:1:1 mixture of saturated ammonium chloride:brine:water. The layers were separated and the aqueous phase extracted with methylene chloride (3×25 ml). The combined organic phase and methylene chloride extracts were dried over magnesium sulfate, filtered and distilled at atmospheric pressure to remove the solvents. The residue was then distilled at reduced pressure (20 mmHg) using a Vigreaux column to give ethyl 3-hydroxy-2-methyl-4,4,4-trifluorobutanoate, bp 78-84° C., 20 mmHg.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06130315
出典データセットuspto-grants-2000_10
ORD IDord-17d7ea44ea634f2fbf32a772f4911a8c
出典メモuspto-grants-2000_10