HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tributylstannane → HCID 14311457, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tributylstannane | HCID 5948 | — |
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | HCID 53939166 | HCID 53939166 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 14311457 | HCID 14311457 | — |
Reaction Steps
To a solution of the crude methyl 2,3,6-tri-O-benzoyl-4-(methylthio)thiocarbonyl-α-D-glucopyranoside (5.70 g, 9.55 mmol) in 120 mL of dry toluene was added AIBN (50 mg). Tributyl tin hydride (6.68 mL, 24.8 mmol) was added and the reaction was heated to reflux for 4 hours. The toluene was removed under reduced pressure. Acetonitrile (200 mL) was added and the mixture extracted with petroleum ether (5×100 mL) to remove all tin salts. After drying over anhydrous sodium sulfate, the solvent was removed under reduced pressure to yield a clear colorless oil which solidified on standing. Purification by flash column chromatography using 20% ethyl acetate in petroleum ether as the eluant gave the target compound as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05811512 |
| Source dataset | uspto-grants-1998_09 |
| ORD ID | ord-c4d1f7da4ea249d1a3eee4e61b3912db |
| Source note | uspto-grants-1998_09 |