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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 400630생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/400630

반응식

참여 물질

역할이름HCID투입량
반응물Cesium fluorideHCID 25953—
반응물Tetrabutylammonium FluorideHCID 2724141—
반응물3-(5-Fluoro-2-methoxyphenyl)-3-methylbutyraldehydeHCID 57809896—
반응물(1-Fluorovinyl)dimethylphenylsilaneHCID 60026366—
용매Acetic AcidHCID 176—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물2-Fluoro-5-(5-fluoro-2-methoxyphenyl)-5-methylhex-1-en-3-olHCID 6002661059.9%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08741897B2
출처 데이터셋uspto-grants-2014_06
ORD IDord-9cdcad5474b1446cbfeac0a9d9ddc0cf
출처 메모uspto-grants-2014_06