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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 556775Generated: October 30, 2026

Ethanethiol → HCID 11361588, compound

https://huagongshe.com/reaction/556775

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanethiolHCID 6343—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 66765654HCID 66765654—
SolventDichloromethaneHCID 6344—
ProductHCID 11361588HCID 1136158864.6%

Reaction Steps

To a mixture of 5-(2,3,4,6-tetra-O-benzyl-β-D-glucopyranosyl)-3-(2-phenylethyl)benzo[b]thiophene (0.1 g) and ethanethiol (0.16 g) in dichloromethane (6 mL) was added boron trifluoride diethyl ether complex (0.28 g) at room temperature, and the mixture was stirred at room temperature for 3 hours. A saturated potassium carbonate aqueous solution was added to the reaction mixture, and the mixture was extracted with ethylacetate. The organic layer washed with brine and dried over anhydrous magnesium sulfate, and the solvent was removed under reduced pressure. The residue was purified by column chromatography on silica gel (eluent: dichloromethane/methanol=10/1-5/1) to give the title compound (0.034 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08058245B2
Source datasetuspto-grants-2011_11
ORD IDord-584cb2296b4c4bafa4d01b1ec7659f67
Source noteuspto-grants-2011_11