戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1019346作成日:2026年10月27日

Cyclopropyl methyl ketone → 1-Cyclopropyl-3-(2-methylthio-4-trifluoromethylphenyl)-1,3-propanedione

https://huagongshe.com/reaction/1019346

反応式

関与物質

役割名称HCID仕込み量
反応物Cyclopropyl methyl ketoneHCID 13004—
反応物Sodium MethoxideHCID 10942334—
反応物Methyl 2-(methylthio)-4-(trifluoromethyl)benzoateHCID 10944828—
溶媒ChlorobenzeneHCID 7964—
生成物1-Cyclopropyl-3-(2-methylthio-4-trifluoromethylphenyl)-1,3-propanedioneHCID 1112017899.3%

反応条件

温度75 °C

反応手順

Sodium methoxide (64 g, 1.15M) was added to a mixture of methyl 2-methylthio-4-trifluoromethylbenzoate (200 g, 0.8M) in chlorobenzene (380 g). The mixture was heated to 75° C. and cyclopropyl methyl ketone (75 g, 0.88M) added during 2 hours whilst maintaining stirring at 75° C. After 4 hours methanol was distilled under reduced pressure. the mixture cooled to 50° C., and water followed by sulphuric acid (53 g of 36N) added. The organic phase was distilled under reduced pressure to give 1-cyclopropyl-3-(2-methylthio-4-trifluoromethylphenyl)propane-1,3-dione as yellow crystals (240 g), m.p. 58-60° C. A yield of 88% was obtained. The purity of the product was 90%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06486356B2
出典データセットuspto-grants-2002_11
ORD IDord-bf69f87a0bd1485ab4273d94effa8768
出典メモuspto-grants-2002_11