Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | HCID 68878932 | HCID 68878932 | — |
| Product | HCID 131727774 | HCID 131727774 | — |
Reaction Steps
The [3-fluoro-4-(3-methoxy-phenoxy)-benzyl]-(3-methyl-butyl)-amine (460 mg, 1.45 mmol) was dissolved in dichloromethane (10 ml) and cooled to −78° C. as boron tribromide (7.25 mL of a 1.0 M in dichloromethane, 7.25 mmol) was added slowly. After 1 hour at −78° C., the reaction was allowed to warm to room temperature. After 4 hours at room temperature the reaction mixture was carefully being quenched with cold water before the pH was adjusted to 10.0 using concentrated ammonium hydroxide. The reaction mixture was extracted with dichloromethane two times and the combined organic layers were washed with brine, dried over sodium sulfate, filtered, and concentrated. The residue was purified by preparative thin layer chromatography on silica eluting with 5% methanol in ethyl acetate. The HCl salt of the product thus isolated was formed by dissolving the free base in ethyl acetate and adding 1 ml of 4.0 M HCl in dioxane and evaporating to afford the product (2A) a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07618996B2 |
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| Source dataset | uspto-grants-2009_11 |
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| ORD ID | ord-067eec96e98f4d429dc90d5405691528 |
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| Source note | uspto-grants-2009_11 |
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