HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → 4-(3-Benzyloxypropyl)bromobenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 3-(4-Bromophenyl)propan-1-ol | HCID 10560614 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 4-(3-Benzyloxypropyl)bromobenzene | HCID 21909326 | — |
Reaction Steps
A suspension of sodium hydride (60%, 0.97 g), 3-(4-bromophenyl)-1-propanol (1.0 g) and benzyl bromide (0.69 mL) in benzene (24 mL) was stirred for 7 hours under reflux. After cooling to ambient temperature, a saturated aqueous ammonium chloride solution (50 mL) was added to the reaction mixture, and the mixture was extracted with ethyl acetate (100 mL). The organic layer was washed with water (40 mL) and brine (40 mL), and dried over anhydrous sodium sulfate. The solvent was removed under reduced pressure, and the residue was purified by column chromatography on silica gel (eluent: hexane/ethyl acetate=20/1) to give 4-(3-benzyloxypropyl)bromobenzene (1.4 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07465712B2 |
| Source dataset | uspto-grants-2008_12 |
| ORD ID | ord-b7ac4fd27b1e45c5a1e80a0f280b7e80 |
| Source note | uspto-grants-2008_12 |