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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 6061생성일: 2026년 10월 24일

Tetrabutylammonium Fluoride Trihydrate → benzyl (2S,3S,5R)-2-hexyl-3-hydroxy-5-[(tetrahydro-2H-pyran-2-yl)oxy]hexadecanoate

https://huagongshe.com/ko/reaction/6061

반응식

참여 물질

역할이름HCID투입량
반응물Tetrabutylammonium Fluoride TrihydrateHCID 11726816—
반응물benzyl (2S,3S,5R)-2-hexyl-3-[(t-butyldimethylsilyl)oxy]-5-[(tetrahydro-2H-pyran-2-yl)oxy]hexadecanoateHCID 67935903—
용매TetrahydrofuranHCID 8028—
생성물benzyl (2S,3S,5R)-2-hexyl-3-hydroxy-5-[(tetrahydro-2H-pyran-2-yl)oxy]hexadecanoateHCID 6793591460.4%

반응 단계

M)g) 480 mg benzyl (2S,3S,5R)-2-hexyl-3-[(t-butyldimethylsilyl)oxy]-5-[(tetrahydro-2H-pyran-2-yl)oxy]hexadecanoate and 350 mg of tetrabutylammonium fluoride trihydrate were dissolved in 8 ml of THF and stirred for 12 hours. After evaporation the residue was dissolved in 50 ml of ether and washed with water. The ethereal phase was dried and evaporated. The product was chromatographed on silica gel. There was obtained 240 mg of benzyl (2S,3S,5R)-2-hexyl-3-hydroxy-5-[(tetrahydro-2H-pyran-2-yl)oxy]hexadecanoate, MS: 463 [(M+H)+ -dihydro-2H-pyran-2-yl].

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05246960
출처 데이터셋uspto-grants-1993_09
ORD IDord-d4da2a89a30143c9af8c5932f42a6311
출처 메모uspto-grants-1993_09