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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2410404Generated: October 26, 2026

Imidazole → 5-O-[tert-butyl(diphenyl)silyl]-D-arabinofuranose

https://huagongshe.com/reaction/2410404

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantD-ArabinoseHCID 66308—
Reactanttert-ButyldiphenylchlorosilaneHCID 94078—
SolventDimethylformamideHCID 6228—
Product5-O-[tert-butyl(diphenyl)silyl]-D-arabinofuranoseHCID 67182660—

Reaction Steps

D-Arabinose (200 g) and imidazole (199 g) were placed in a three-neck round bottom flask and connected to high vacuum for 30 minutes. The vacuum was released under nitrogen atmosphere and dimethylformamide (1.8 L) was added to the above mixture at room temperature followed by drop-wise addition of t-butyldiphenylchlorosilane (443 mL) for 10 minutes under a nitrogen atmosphere. The resulting mixture was stirred for 16 hours at the same temperature. Dimethylformamide was evaporated under reduced pressure. The residue was taken up in ethyl acetate and washed with water. The organic layer was dried over anhydrous sodium sulphate. The solvent was evaporated under reduced pressure to obtain a crude residue which was purified by column chromatography over silica gel using 80% ethyl acetate in hexane as eluant to afford the title compound (273 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08816073B2
Source datasetuspto-grants-2014_08
ORD IDord-dad2f66104ee4d1a96343fae72ffa4e0
Source noteuspto-grants-2014_08