HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Bromo-4-fluorobenzene → 3-((4-Bromophenoxy)methyl)oxetane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Bromo-4-fluorobenzene | HCID 9993 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Oxetan-3-ylmethanol | HCID 11521066 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-((4-Bromophenoxy)methyl)oxetane | HCID 60169428 | 15.3% |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
To a solution of oxetan-3-ylmethanol (1.00 g, 11.3 mmol) in DMF (10 mL) was added NaH (300 mg, 13.6 mmol) at 0° C. The mixture was then stirred at 0° C. for 10 min. 1-Bromo-4-fluorobenzene (2.30 g, 13.6 mmol) was added to the solution. The mixture was stirred at 90° C. for 2 h. The mixture was partitioned between water and EtOAc (30 mL×3). The combined organics was dried and concentrated to give the title compound (420 mg, 15% yield) as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08889730B2 |
| Source dataset | uspto-grants-2014_11 |
| ORD ID | ord-69e6a41085fa4b72ad4a85dc696e6760 |
| Source note | uspto-grants-2014_11 |