HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → HCID 54410149, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Dibutyltin oxide | HCID 61221 | — |
| Reactant | 4-Nitrophenylgalactoside | HCID 65115 | — |
| Reactant | Ammonia methanol dichloromethane | HCID 21584172 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 54410149 | HCID 54410149 | — |
Reaction Steps
Dibutyltin oxide (1.87 g, 7.5 mmol) is added to a solution of p-nitrophenyl β-D-galactopyranoside (1.5 g, 5.0 mmol) in absolute dioxane (40 ml) and the mixture is heated under reflux. After 3 hours, benzyl bromide (3.6 ml, 30 mmol) are added to the solution obtained and the batch is stirred under reflux for a further 48 hours. The solvent is then distilled off in vacuo and the residue is purified by flash chromatography (ethyl acetate/petroleum ether 2:1→1:1]. Colourless crystals (1.58 g 81%) are obtained; TLC [methylene chloride/methanol/ammonia (25%) 15:3:0.2]: Rf=0.69; melting point=127° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06271342B1 |
| Source dataset | uspto-grants-2001_08 |
| ORD ID | ord-826400f6b42845ec96024794699721ca |
| Source note | uspto-grants-2001_08 |