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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1154653Generated: November 2, 2026

Chloroform → HCID 13316668, compound

https://huagongshe.com/reaction/1154653

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroformHCID 6212—
ReactantAllyl bromideHCID 7841—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 13316665HCID 13316665—
ProductHCID 13316668HCID 13316668—

Reaction Steps

3.1 gm (0.007 mol) of 1-[7,8-dimethoxy-1,3,4,5-tetrahydro-2H-3-benzazepin-2-on-3-yl]-3-[N-(2-{3,4-dimethoxy-phenyl}-ethyl)-amino]-propane were refluxed for 21 hours with 1.0 gm (0.007 mol) of potassium carbonate and 0.6 ml (0.007 mol) of allyl bromide in 100 ml of chloroform. Subsequently, the organic phase was extracted with water, dried, evaporated in vacuo, and the residue was purified on an aluminum oxide column (300 gm neutral, activity III) with methylene chloride containing 2% of acetone as the eluant. Subsequently the hydrochloride was precipitated.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04490369
Source datasetuspto-grants-1984_12
ORD IDord-9fecd3d26ad246afb75b32c5f45992c5
Source noteuspto-grants-1984_12