HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanethiol → HCID 11361588, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanethiol | HCID 6343 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 66765654 | HCID 66765654 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 11361588 | HCID 11361588 | 64.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08058245B2 |
| Source dataset | uspto-grants-2011_11 |
| ORD ID | ord-584cb2296b4c4bafa4d01b1ec7659f67 |
| Source note | uspto-grants-2011_11 |