HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanethiol → 2-(beta-D-Glucopyranosyl)-4-(2-phenylethyl)benzo[b]thiophene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanethiol | HCID 6343 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-(2,3,4,6-tetra-O-benzyl-beta-D-glucopyranosyl)-4-(2-phenylethyl)benzo[b]thiophene | HCID 68718338 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(beta-D-Glucopyranosyl)-4-(2-phenylethyl)benzo[b]thiophene | HCID 11361587 | 30.8% |
Reaction Steps
To a solution of 2-(2,3,4,6-tetra-O-benzyl-β-D-glucopyranosyl)-4-(2-phenylethyl)benzo[b]thiophene (0.58 g) and ethanethiol (1.13 mL) in dichloromethane (10 mL) was added boron trifluoride diethyl ether complex (1.43 mL) at room temperature, and the mixture was stirred for 3 hours. A saturated potassium carbonate aqueous solution was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The extract 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) to give the title compound (94 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07732596B2 |
| Source dataset | uspto-grants-2010_06 |
| ORD ID | ord-d242b309769541cd9bdfd13e8f2903ab |
| Source note | uspto-grants-2010_06 |