Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 916602Generated: November 2, 2026

Bromotrimethylsilane → HCID 69015383, compound

https://huagongshe.com/reaction/916602

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromotrimethylsilaneHCID 76113—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 69422865HCID 69422865—
SolventDichloromethaneHCID 6344—
ProductHCID 69015383HCID 6901538316.4%

Reaction Steps

To a solution of 2-(β-D-glucopyranosyloxy)-3-[4-(2-methoxymethyloxyethyl)benzyl]-4,6-dimethylpyridine (0.054 g) in dichloromethane (1.2 mL) was trimethylbromosilane (0.061 mL) at −23° C., and the mixture was stirred for 10 minutes. To the reaction mixture was added saturated aqueous sodium bicarbonate solution, and the mixture was extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate, and the solvent was removed under reduced pressure. The residue was purified by preparative thin layer chromatography on silica gel (developing solvent: dichloromethane/methanol=6/1) to give 2-(β-D-glucopyranosyloxy)-3-[4-(2-hydroxyethyl)benzyl]-4,6-dimethylpyridine (0.008 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07271153B2
Source datasetuspto-grants-2007_09
ORD IDord-0a697495cf2a4108bc728aaac11cae4b
Source noteuspto-grants-2007_09