Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | HCID 68428691 | HCID 68428691 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 68430082 | HCID 68430082 | 79% |
Reaction Steps
To a mixture of lithium aluminum hydride (0.061 g) and diethyl ether (2.0 mL) was added a solution of the compound obtained in step 1 (0.35 g) in diethyl ether (3.0 mL), and the resulting mixture was stirred at room temperature for 2 hr under a nitrogen atmosphere. 1N Aqueous sodium hydroxide solution (0.061 mL), saturated aqueous ammonium chloride (0.061 mL) and water (0.061 mL) were added, and the resulting mixture was stirred at room temperature for 3 hr. The precipitate was removed by filtration, and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (25% ethyl acetate/hexane) to give 4-benzyl-8-(isopropylthio)-2,3,4,5-tetrahydropyrido[3,2-f][1,4]oxazepine (0.26 g, 79%) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08329687B2 |
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| Source dataset | uspto-grants-2012_12 |
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| ORD ID | ord-a635f8db3ea7455f8a8918f5599077b7 |
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| Source note | uspto-grants-2012_12 |
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