HuagongsheHuagongshe Chemistry Print Report · For research reference only
Boron tribromide → [4-(2-Azepan-1-yl-ethoxy)-phenyl][2-(2,5-difluorophenyl)-6-hydroxynaphthalen-1-yl]-methanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Chloroform isopropyl alcohol | HCID 21906603 | — |
| Reactant | [4-(2-Azepan-1-yl-ethoxy)-phenyl]-[2-(2,5-difluoro-phenyl)-6-methoxy-naphthalen-1-yl]-methanone | HCID 57552524 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | [4-(2-Azepan-1-yl-ethoxy)-phenyl][2-(2,5-difluorophenyl)-6-hydroxynaphthalen-1-yl]-methanone | HCID 67004614 | 46.1% |
Reaction Steps
Dissolve [4-(2-azepan-1-yl-ethoxy)-phenyl]-[2-(2,5-difluoro-phenyl)-6-methoxy-naphthalen-1-yl]-methanone (1.74 g, 3.37 mmol) in 20 mL methylene chloride and chill in ice. Add to this solution 2.0 mL of boron tribromide (5.3 g, 21.2 mmol) and allow to come to room temperature. Pour into a two phase solution of saturated sodium bicarbonate and 3/1 chloroform/isopropanol. Separate the organic layer, wash with water and dry over 3 Å sieves. Evaporate the solvent and purify on a silica gel column eluting with a 0-10% methanol/methylene chloride gradient. Evaporate the solvent to yield 780 mg (46%) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08217032B2 |
| Source dataset | uspto-grants-2012_07 |
| ORD ID | ord-f08f20ce183c4dc3adaef2f5ab105011 |
| Source note | uspto-grants-2012_07 |