Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 218979Generated: October 29, 2026

Triethylsilane → HCID 59426851, compound

https://huagongshe.com/reaction/218979

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylsilaneHCID 12052—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 68587617HCID 68587617—
SolventAcetonitrileHCID 6342—
ProductHCID 59426851HCID 5942685131.3%

Reaction Conditions

Temperature-20 °C

Reaction Steps

To an acetonitrile (5.0 ml) solution of 1-C-{3-[1-benzothien-2-yl(hydroxy)methyl]-4-fluorophenyl}-2,3,4,6-tetra-O-benzyl-D-glucopyranose (500 mg) were added triethylsilane (175 mg) and boron trifluoride-diethyl ether complex (196 mg) in an argon atmosphere at −20° C., followed by stirring at −20° C. for 5 hours. To the reaction mixture was added a saturated aqueous sodium bicarbonate solution, followed by extraction with chloroform. The organic layer was washed with a saturated aqueous sodium bicarbonate solution and a saturated aqueous sodium chloride solution, dried over anhydrous magnesium sulfate, filtered and concentrated. The residue was purified by silica gel column chromatography (n-hexane/ethyl acetate) to obtain (1S)-1,5-anhydro-1-[3-(1-benzothien-2-ylmethyl)-4-fluorophenyl]-2,3,4,6-tetra-O-benzyl-D-glucitol (150 mg, yield: 30.2%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08198464B2
Source datasetuspto-grants-2012_06
ORD IDord-a94f709b941847ee8e2b7bd19ab04985
Source noteuspto-grants-2012_06