HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → Benzene, [(3-butenyloxy)methyl]-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 3-Buten-1-ol | HCID 69389 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Benzene, [(3-butenyloxy)methyl]- | HCID 10441993 | — |
Reaction Steps
NaH (0.24 g) was slowly added to a solution of 3-buten-1-ol (0.72 g) in DMF (15 ml) at 0° C., and the reaction stirred for 30 minutes. Benzyl bromide (1.9 g) was added and the reaction was stirred at 25° C. for 18 hours. The mixture was filtered and concentrated. The residue was dissolved in hexane, washed with water (3×), dried over MgSO4, and concentrated. Purification by chromatography over silica gel (5% ethyl ether in hexane) afforded the titled compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05120729 |
| Source dataset | uspto-grants-1992_06 |
| ORD ID | ord-6d5db8413a574664994feed5ea874261 |
| Source note | uspto-grants-1992_06 |