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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1077658생성일: 2026년 10월 26일

Tetrabutylammonium Fluoride → 4-[(5,6,7,8-Tetrahydro-5-hydroxy-8,8-dimethyl-5-carboethoxymethylnaphth-2-yl)ethynyl]benzoic acid

https://huagongshe.com/reaction/1077658

반응식

참여 물질

역할이름HCID투입량
반응물Tetrabutylammonium FluorideHCID 2724141—
반응물Trimethylsilylethyl 4-((5,6,7,8-tetrahydro-5-hydroxy-8,8-dimethyl-5-carboethoxy-methylnaphth-2-yl)ethynyl]benzoateHCID 70151178—
용매TetrahydrofuranHCID 8028—
생성물4-[(5,6,7,8-Tetrahydro-5-hydroxy-8,8-dimethyl-5-carboethoxymethylnaphth-2-yl)ethynyl]benzoic acidHCID 18314566—

반응 단계

To a solution of 0.25 g (0.49 mmol) of trimethylsilylethyl 4-[(5,6,7,8-tetrahydro-5-hydroxy-8,8-dimethyl-5-carboethoxy-methylnaphth-2-yl)ethynyl]benzoate (Compound 117) in 5 ml of dry THF (flushed with argon) was added 1.48 ml (1.5 mmol) of tetrabutyl ammonium fluoride (1M solution in THF). The reaction mixture was stirred at room temperature for 12 hours, concentrated in vacuo to an oil and slowly diluted with water. The solution was acidified to pH 4 with 10% HCl and extracted with Et2O. The organic layer was dried over Na2SO4, concentrated in vacuo to an oil and purified by flash chromatography (silica, 90% EtOAc-hexane) to give the title compound as a white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05543534
출처 데이터셋uspto-grants-1996_08
ORD IDord-76ca9c5403f84b51b54b47488e72bdbb
출처 메모uspto-grants-1996_08