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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 3841Generated: October 26, 2026

Triethylamine → 1-Cinnamyl-4-(3-chloropropyl)piperazine dihydrochloride

https://huagongshe.com/reaction/3841

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantBromomethylstyreneHCID 98116—
ReactantBis(1-(3-chloropropyl)piperazine);hydrate;tetrahydrochlorideHCID 131714940—
SolventEthanolHCID 702—
Product1-Cinnamyl-4-(3-chloropropyl)piperazine dihydrochlorideHCID 70415497278.1%

Reaction Steps

6.0 g of cinnamyl bromide were added to a mixture of 7.4 g of 1-(3-chloropropyl)piperazine dihydrochloride hemihydrate, 6.1 g of triethylamine and 100 ml of reagent ethanol. The mixture was refluxed for 4 hours and then stirred overnight. After removal of the solvent in vacuo, water was added to the residue. The product was then extracted with ether and the extract was dried (magnesium sulfate) and concentrated. The resulting oil was chromatographed on silica gel (methylene chloride/methanol: 9/1) and precipitated with ethereal hydrochloric acid to give 7.4 g (70% of theory) of 1-cinnamyl-4-(3-chloropropyl)piperazine dihydrochloride.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04722926
Source datasetuspto-grants-1988_02
ORD IDord-d30d8a19d77a43a283a0480973ee3168
Source noteuspto-grants-1988_02