HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → HCID 54325576, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 4-(2-Carboxyethyl)-4-nitroheptanedioic acid | HCID 2801600 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 54325576 | HCID 54325576 | 82.2% |
Reaction Steps
To a mixture of [3-(2-carboxyethyl)]-3-nitropentane-1,5-dicarboxylic acid (2.8 g, 0.01 mole) (prepared as described by James K. Young et al., Macromolecules, 1994, 27, 3464-34-71) and cesium carbonate (3.25 g, 0.025 mol) in acetonitrile (20.0 mL) was added benzylbromide (8.55 g, 6.0 mL, 0.05 mole) and the mixture stirred at RT for 24 h. Inorganic salts were filtered and the salts washed with acetonitrile. The filtrate and the washings were combined and evaporated to obtain an oil. Purification by chromatography over silica gel (hexane:ethyl acetate, 7:3) afforded the benzyl ester (40) as colorless viscous oil (4.5 g, yield: 82%). Mass Spectrum (M+H)+ =548.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06093382 |
| Source dataset | uspto-grants-2000_07 |
| ORD ID | ord-16fa941f968b4839a2e378a72cc8ecf3 |
| Source note | uspto-grants-2000_07 |