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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1653866Generated: November 3, 2026

Allyl bromide → 2-allyl-8-methoxy-2,3,4,5-tetrahydro-1H-2-benzazepin-1-one

https://huagongshe.com/reaction/1653866

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
Reactant8-Methoxy-2,3,4,5-tetrahydro-benzo[c]azepin-1-oneHCID 11275529—
SolventDimethylformamideHCID 6228—
SolventSodium chloride; waterHCID 57417360—
Product2-allyl-8-methoxy-2,3,4,5-tetrahydro-1H-2-benzazepin-1-oneHCID 2290499883%

Reaction Steps

A solution of 8-methoxy-2,3,4,5-tetrahydro-1H-2-benzazepin-1-one (10.0 g, 0.052 mol) in N,N-dimethylformamide (30 mL) and allylbromide (23 mL, 0.260 mL) was treated with Nail (60% by wt. dispersion in oil, 2.50 g, 0.063 mol) and the resulting grey suspension stirred at room temperature under an atmosphere of argon. Gas evolution was noted. After 15 minutes, the solution was diluted with brine and partitioned between ethyl acetate and brine. The combined organic layers were concentrated in vacuo and purified by chromatography over silica gel eluting with a gradient of hexane to 1:1 ethyl acetate/hexane to yield 8 g (83%) of 2-allyl-8-methoxy-2,3,4,5-tetrahydro-1H-2-benzazepin-1-one as a colorless oil:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05403836
Source datasetuspto-grants-1995_04
ORD IDord-9e345956436c46d3aba73851644b24b9
Source noteuspto-grants-1995_04