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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantSodium hydrideHCID 24758—
Reactant3-Ethyl-3-(3-benzyloxy-phenyl)-azepan-2-oneHCID 21706301—
SolventDimethylformamideHCID 6228—
Product1-Allyl-3-ethyl-3-(3-benzyloxy-phenyl)-azepan-2-oneHCID 21706306—

Reaction Conditions

Temperature25 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06284755B1
Source datasetuspto-grants-2001_09
ORD IDord-f6481199bb344b32b3a90b4ad3d0ea87
Source noteuspto-grants-2001_09