Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Borane;tetrahydrofuran | HCID 2723981 | — |
| Reactant | HCID 68578555 | HCID 68578555 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 25122709 | HCID 25122709 | 59.5% |
Reaction Steps
To a solution of 4-benzyl-7-bromo-3,4-dihydro-1,4-benzoxazepine-5 (2H)-one (4.20 g, 12.8 mmol) in tetrahydrofuran (400 ml) was added 1M borane-tetrahydrofuran solution (52.8 ml, 52.8 mmol) and the mixture was stirred at 80° C. for 2 hr. Under ice-cooling, methanol (240 ml) and sodium hydroxide (20.8 g, 519 mmol) were added, and the mixture was stirred at room temperature for 2 hr. The solvent was evaporated under reduced pressure. The residue was poured into water and the mixture was extracted with ethyl acetate. The extract was dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=1:1) to give the desired product (2.42 g, 59.5%) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08247403B2 |
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| Source dataset | uspto-grants-2012_08 |
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| ORD ID | ord-a5c83f201af04d2188b8b38aca4a3587 |
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| Source note | uspto-grants-2012_08 |
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