HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1594913Generated: October 30, 2026
Allyl bromide → 1-Allyl-3-ethyl-3-(3-benzyloxy-phenyl)-azepan-2-one
https://huagongshe.com/reaction/1594913
Participants
| Role | Name | HCID | Charge |
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| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 3-Ethyl-3-(3-benzyloxy-phenyl)-azepan-2-one | HCID 21706301 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-Allyl-3-ethyl-3-(3-benzyloxy-phenyl)-azepan-2-one | HCID 21706306 | — |
Reaction Steps
To a solution of 3-ethyl-3-(3-benzyloxy-phenyl)-azepan-2-one, as described above in Step A, (1.65 g, 5.1 mmol) in DMF (25 mL) at 0° C. was added NaH (0.265 g, 6.63 mmol) and the mixture was stirred for 20 min at 0° C. and 20 min at 25° C. Allyl bromide (0.66 mL, 7.65 mmol) was added. After 5 hr, additional NaH (0.13 g, 3 mmol) and allyl bromide (0.33 mL, 3.5 mmol) were added and stirring was continued for 16 hr. The reaction was quenched with H2O and the solvents removed in vacuo . The residue was partitioned between EtOAc and saturated NaHCO3 solution. The organic layer was separated, washed with brine and dried (MgSO4). Filtration and concentration gave the title compound after chromatography on silica gel with hexane and ethyl acetate 9:1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06284755B1 |
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| Source dataset | uspto-grants-2001_09 |
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| ORD ID | ord-f6481199bb344b32b3a90b4ad3d0ea87 |
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| Source note | uspto-grants-2001_09 |
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