戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 400630作成日:2026年10月27日

Cesium fluoride → 2-Fluoro-5-(5-fluoro-2-methoxyphenyl)-5-methylhex-1-en-3-ol

https://huagongshe.com/reaction/400630

反応式

関与物質

役割名称HCID仕込み量
反応物Cesium fluorideHCID 25953—
反応物Tetrabutylammonium FluorideHCID 2724141—
反応物3-(5-Fluoro-2-methoxyphenyl)-3-methylbutyraldehydeHCID 57809896—
反応物(1-Fluorovinyl)dimethylphenylsilaneHCID 60026366—
溶媒Acetic AcidHCID 176—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
溶媒Ethyl AcetateHCID 8857—
生成物2-Fluoro-5-(5-fluoro-2-methoxyphenyl)-5-methylhex-1-en-3-olHCID 6002661059.9%

反応手順

To a solution of 3-(5-fluoro-2-methoxyphenyl)-3-methylbutyraldehyde (1.1 g, 5.2 mmol) and the above (1-fluorovinyl)dimethylphenylsilane (2.2 g, 12.2 mmol) in 5 mL of THF was added 0.6 mL of tetrabutylammonium fluoride (1 M in THF) and the mixture was stirred at room temperature overnight. TLC showed partial conversion to product. Cesium fluoride (0.22 g) was added and the mixture was stirred at room temperature for 3 days. 2 mL of water and 2 mL of acetic acid were added and the mixture was warmed at 60° C. for 2 hours to effect desilylation of any silylated product. The mixture was diluted with ethyl acetate, washed with water, dried, filtered and concentrated in vacuo. Fractionation of the residue over silica gel (eluent: hexanes-dichloromethane (3:1 to 1:3 gradient) gave 0.798 g (59.5% yield) of 2-fluoro-5-(5-fluoro-2-methoxyphenyl)-5-methylhex-1-en-3-ol as an oil which was used without additional purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08741897B2
出典データセットuspto-grants-2014_06
ORD IDord-9cdcad5474b1446cbfeac0a9d9ddc0cf
出典メモuspto-grants-2014_06