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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1531579Generated: October 30, 2026

Tributylstannane → HCID 14311457, compound

https://huagongshe.com/reaction/1531579

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributylstannaneHCID 5948—
ReactantAzobisisobutyronitrileHCID 6547—
ReactantHCID 53939166HCID 53939166—
SolventTolueneHCID 1140—
ProductHCID 14311457HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06197963B1
Source datasetuspto-grants-2001_03
ORD IDord-e0ad86e5f1ce4a5597eb687f002371b8
Source noteuspto-grants-2001_03