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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 6256Erstellt: 23. Oktober 2026

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

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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
EduktImidazoleHCID 795—
Edukttert-ButyldiphenylchlorosilaneHCID 94078—
Edukt(R)-3-(benzyloxy)propane-1,2-diolHCID 2724795—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt(S)-1-Benzyloxy-3-(t-butyldiphenylsilyloxy)propan-2-olHCID 1098269890%

Reaktionsschritte

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%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05247085
Quelldatensatzuspto-grants-1993_09
ORD IDord-cf9e57ba9a5d488b84ad34a0e5f55896
Quellennotizuspto-grants-1993_09