HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Bromo-3-methylbutane → 1-Bromo-4-[(3-methylbutoxy)methyl]benzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Bromo-3-methylbutane | HCID 7891 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 4-Bromobenzyl alcohol | HCID 70119 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-Bromo-4-[(3-methylbutoxy)methyl]benzene | HCID 58452284 | 85% |
Reaction Steps
Sodium hydride (purity: 55%, 700 mg) and 1-bromo-3-methylbutane (2.56 mL) were added to a solution of 4-bromobenzylalcohol (2.0 g) in N,N-dimethylformamide (40 mL) under ice-cooling, and the mixture was stirred at room temperature for five hours. A saturated ammonium chloride solution was added to the reaction solution, followed by extraction with a mixture of hexane-ethyl acetate (1:1). The organic layer was dried over sodium sulfate and filtered. The solvent was then evaporated under reduced pressure. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=100:1→50:1→30:1) to give the title compound (2.31 g, 85%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08822503B2 |
| Source dataset | uspto-grants-2014_09 |
| ORD ID | ord-0119a32b104e4da9b9562b6b942d0ba1 |
| Source note | uspto-grants-2014_09 |