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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 703687생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/703687

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

480 mg of benzyl (2S,3S,5R)-2-hexyl-3-[(t-butyl-dimethylsilyl)oxy]-5 -[(tetrahydro-2H-pyran-2-yl)oxy]hexadecanoate and 350 mg of tetrabutylammonium fluoride trihydrate are dissolved in 8 ml of THF and stirred for 12 hours. After evaporation the residue is dissolved in 50 ml of ether and washed with water. The ethereal phase is dried and evaporated. The crude product is chromatographed on silica gel. There are 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 번호US04983746
출처 데이터셋uspto-grants-1991_01
ORD IDord-7ebec7ebb6004bc180167b4dc1b4b8e3
출처 메모uspto-grants-1991_01