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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 15412Generated: October 29, 2026

Ethanethiol → 2-(beta-D-Glucopyranosyl)-7-(4-methylbenzyl)benzo[b]thiophene

https://huagongshe.com/reaction/15412

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanethiolHCID 6343—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 68714543HCID 68714543—
SolventDichloromethaneHCID 6344—
Product2-(beta-D-Glucopyranosyl)-7-(4-methylbenzyl)benzo[b]thiopheneHCID 1174995232%

Reaction Steps

To a solution of 2-(2,3,4,6-tetra-O-benzyl-β-D-glucopyranosyl)-7-(4-methylbenzyl)benzo[b]thiophene (0.95 g) and ethanethiol (1.8 mL) in dichloromethane (15 mL) was added boron trifluoride diethyl ether complex (2.1 mL) at room temperature. The reaction mixture was stirred at room temperature for 3 hours, and a saturated potassium carbonate aqueous solution was added to the mixture. The mixture was extracted with ethyl acetate. The organic layer washed with brine and dried over anhydrous magnesium sulfate. The solvent was removed under reduced pressure, and the residue was purified by column chromatography on silica gel (eluent: dichloromethane/methanol=10/1) to give the title compound (0.16 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07732596B2
Source datasetuspto-grants-2010_06
ORD IDord-a0615df7fb9943238736a4156d6b0da8
Source noteuspto-grants-2010_06