HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 515444Generated: October 26, 2026
4-Benzyl-5-methyl-[1,4]oxazepan-3-one → 4-Benzyl-5-methyl-[1,4]oxazepane
https://huagongshe.com/reaction/515444
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Benzyl-5-methyl-[1,4]oxazepan-3-one | HCID 58405253 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-Benzyl-5-methyl-[1,4]oxazepane | HCID 66718790 | 100% |
Reaction Steps
To a solution of 4-benzyl-5-methyl-[1,4]oxazepan-3-one (0.32 g, 1.4 mmol) in tetrahydrofuran (5 mL) was added 1M solution of boran-tetrahydrofran complex in tetrahydrofuran (5 mL, 5.0 mmol) dropwise at 0° C. under nitrogen atmosphere. The mixture was warmed to room temperature and stirred for 3 hours. Then the reaction was quenched by the addition of methanol and the solution was concentrated. The residual oil was dissolved in methanol (10 mL) and 1M sodium hydroxide aqueous solution was added at room temperature. The mixture was refluxed for 3 hours and diluted with water. Extraction with ethyl acetate was performed and the organic extracts were dried over anhydrous sodium sulfate. After evaporation of solvents, the residue was purified by flash column chromatography on silica gel to yield 4-benzyl-5-methyl-[1,4]oxazepane (0.30 g, 1.4 mmol, 100%) as colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09108957B2 |
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| Source dataset | uspto-grants-2015_08 |
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| ORD ID | ord-5dce31e93ef24052b61c4d955ee83513 |
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| Source note | uspto-grants-2015_08 |
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