HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanethiol → 2-(beta-D-Glucopyranosyl)-7-(4-methylbenzyl)benzo[b]thiophene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanethiol | HCID 6343 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 68714543 | HCID 68714543 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(beta-D-Glucopyranosyl)-7-(4-methylbenzyl)benzo[b]thiophene | HCID 11749952 | 32% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07732596B2 |
| Source dataset | uspto-grants-2010_06 |
| ORD ID | ord-a0615df7fb9943238736a4156d6b0da8 |
| Source note | uspto-grants-2010_06 |