HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,3-Dibromopropane → [4-(Allyloxy)butyl]benzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,3-Dibromopropane | HCID 8001 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Benzenebutanol | HCID 76889 | — |
| Catalyst | Tetrabutylammonium Bromide | HCID 74236 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | [4-(Allyloxy)butyl]benzene | HCID 67246079 | 250.3% |
Reaction Steps
To a solution of 4-phenylbutan-1-ol (0.60 g, 3.99 mmol) in 1,3-dibromopropane (2.14 mL, 10.60 mmol) was added tetrabutylammonium bromide (20 mg, 0.064 mmol) and 50% sodium hydroxide (1.5 mL). The mixture was stirred at room temperature overnight. The crude reaction was diluted with n-hexane (20 mL) and washed with water (2×10 mL), dried (Na2SO4), and the solvent removed under reduced pressure. The title compound (1.90 g, 92% purity) was obtained by distillation of the residue under reduced pressure and was used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07964615B2 |
| Source dataset | uspto-grants-2011_06 |
| ORD ID | ord-bced35568b9d4c5db89d0627fb1a5948 |
| Source note | uspto-grants-2011_06 |