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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 971605Generated: October 30, 2026

Butyl bromide → HCID 21312832, compound

https://huagongshe.com/reaction/971605

Reaction equation

Participants

RoleNameHCIDCharge
ReactantButyl bromideHCID 8002—
ReactantPotassium HydroxideHCID 14797—
ReactantHCID 12668015HCID 12668015—
SolventMethanolHCID 887—
ProductHCID 21312832HCID 21312832—

Reaction Steps

A mixture of 4.5 g of 6-chloro-7,8-dimethoxy-1-phenyl-2,3,4,5-tetrahydro-1H-3-benzazepine, 0.02 ml of n-butyl bromide and 0.02 mol of potassium hydroxide is dissolved in 120 ml of dry methanol and refluxed for 48 hours. The reaction mixture is evaporated to dryness, taken up in ethyl acetate and filtered to remove inorganic salts. The filtrate is washed with water, dried and evaporated to give 3-n-butyl-6-chloro-7,8-dimethoxy-1-phenyl-2,3,4,5-tetrahydro-1H-3-benzazepine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04160765
Source datasetuspto-grants-1979_07
ORD IDord-12f5ef31036c48bd8c99cd5ee2fa7ee3
Source noteuspto-grants-1979_07