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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1161026생성일: 2026년 10월 25일

Tetrabutylammonium Fluoride → 3-[(4-Hydroxymethyl-phenyl)-(tetrahydro-pyran-2-yloxy)-methyl]-benzonitrile

https://huagongshe.com/reaction/1161026

반응식

참여 물질

역할이름HCID투입량
반응물Tetrabutylammonium FluorideHCID 2724141—
반응물3-[(Tetrahydro-pyran-2-yloxy)-(4-triisopropylsilanyloxymethyl-phenyl)-methyl]-benzonitrileHCID 57438296—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물3-[(4-Hydroxymethyl-phenyl)-(tetrahydro-pyran-2-yloxy)-methyl]-benzonitrileHCID 5743829982%

반응 단계

Add a 1M solution in tetrahydrofuran of tetrabutylammonium fluoride (37 mL, 37 mmol) to a solution of 3-[(tetrahydro-pyran-2-yloxy)-(4-triisopropylsilanyloxymethyl-phenyl)-methyl]-benzonitrile (14.6 g, 30.4 mmol) in tetrahydrofuran (50 mL) and tetrahydrofuran stir at room temperature for 2 hours. Concentrate the reaction, dilute with water (200 mL), and extract with ethyl acetate (2×100 mL). Combine the extracts, dry over magnesium sulfate, filter, and concentrate. Purify the residue via silica chromatography eluting with 9:1 hexanes:ethyl acetate to 1:1 hexanes ethyl acetate to afford the title compound (8.0 g, 82%), as a colorless thick oil. LCMS (m/z) 323 M+1.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07816523B2
출처 데이터셋uspto-grants-2010_10
ORD IDord-92115fe7cc8648f8ba098430e5585d55
출처 메모uspto-grants-2010_10