Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1594902Generated: October 29, 2026

Allyl bromide → 1-Allyl-3-ethyl-3-(3-methoxy-phenyl)-azepan-2-one

https://huagongshe.com/reaction/1594902

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantSodium hydrideHCID 24758—
Reactant3-Ethyl-3-(3-methoxyphenyl)azepan-2-oneHCID 2815455—
SolventDimethylformamideHCID 6228—
Product1-Allyl-3-ethyl-3-(3-methoxy-phenyl)-azepan-2-oneHCID 21706279—

Reaction Conditions

Temperature25 °C

Reaction Steps

To a solution of 3-ethyl-3-(3-methoxy-phenyl)-azepan-2-one (as described in Example 8, Step A) (2.62 g, 10.6 mmol) in DMF (20 mL) at 0° C. was added NaH (0.47 g, 11.6 mmol) and the mixture was stirred for 20 min at 0° C. and 20 min at 25° C. Allyl bromide (1.1 mL, 12.7 mmol) was added. After 5 hr, additional NaH (0.12 g, 3 mmol) and allyl bromide (0.3 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-850b7ba9878647a99641335f80becfe6
Source noteuspto-grants-2001_09