HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,6-Dibromohexane → {4-((6-Bromohexyl)oxy]-3,3-difluorobutyl}benzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,6-Dibromohexane | HCID 12368 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2,2-Difluoro-4-phenylbutan-1-ol | HCID 18425775 | — |
| Catalyst | Tetrabutylammonium Bromide | HCID 74236 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | {4-((6-Bromohexyl)oxy]-3,3-difluorobutyl}benzene | HCID 67246468 | — |
Reaction Steps
To a solution of Intermediate 2 (0.60 g, 3.22 mmol) in 1,6-dibromohexane (1.74 mL, 11.27 mmol) was added tetrabutylammonium bromide (21 mg, 0.064 mmol) and 50% sodium hydroxide (1.2 mL). The mixture was stirred at room temperature overnight. The crude reaction was diluted with n-hexane (20 mL), washed with water (2×10 mL), dried (Na2SO4), and the solvent removed under reduced pressure. The title compound was obtained (2.1 g, 52% purity) and was used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08242177B2 |
| Source dataset | uspto-grants-2012_08 |
| ORD ID | ord-cdb17664084b4a9fbb099a70635ba9e3 |
| Source note | uspto-grants-2012_08 |