戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 6061作成日:2026年10月25日

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

https://huagongshe.com/reaction/6061

反応式

関与物質

役割名称HCID仕込み量
反応物Tetrabutylammonium Fluoride TrihydrateHCID 11726816—
反応物benzyl (2S,3S,5R)-2-hexyl-3-[(t-butyldimethylsilyl)oxy]-5-[(tetrahydro-2H-pyran-2-yl)oxy]hexadecanoateHCID 67935903—
溶媒TetrahydrofuranHCID 8028—
生成物benzyl (2S,3S,5R)-2-hexyl-3-hydroxy-5-[(tetrahydro-2H-pyran-2-yl)oxy]hexadecanoateHCID 6793591460.4%

反応手順

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].

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05246960
出典データセットuspto-grants-1993_09
ORD IDord-d4da2a89a30143c9af8c5932f42a6311
出典メモuspto-grants-1993_09