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HRID 6256作成日:2026年10月23日

Acetic Acid → (S)-1-Benzyloxy-3-(t-butyldiphenylsilyloxy)propan-2-ol

https://huagongshe.com/ja/reaction/6256

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物ImidazoleHCID 795—
反応物tert-ButyldiphenylchlorosilaneHCID 94078—
反応物(R)-3-(benzyloxy)propane-1,2-diolHCID 2724795—
溶媒TetrahydrofuranHCID 8028—
生成物(S)-1-Benzyloxy-3-(t-butyldiphenylsilyloxy)propan-2-olHCID 1098269890%

反応手順

To a solution of (R)-3-benzyloxypropane-1,2-diol (prepared from (S)-4-benzylymethyl-2,2-dimethyl-1,3-dioxolane (commercially available from FLUKA) by acid hydrolysis using 80% aqueous acetic acid), (8.3 g, 47.2 mmol) in dry THF (70 ml) was added imidazole (6.42 g, 94.4 mmol). After 2 minutes, t-butyldiphenylsilyl chloride (12.28 ml, 47.2 mmol) was added. A white precipitate formed immediately. After 2 hours, the reaction mixture was filtered and the filtrate evaporated. The residue was partitioned between ethyl acetate and water, the organic layer separated, washed with saturated brine, dried (MgSO4), filtered and evaporated to give a colourless oil. Chromatography of the oil on silica gel (dichloromethane as eluant) afforded the title compound as a colourless oil (17.72 g, 90%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05247085
出典データセットuspto-grants-1993_09
ORD IDord-cf9e57ba9a5d488b84ad34a0e5f55896
出典メモuspto-grants-1993_09