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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1657783Generated: October 31, 2026

Benzene, (3-chloro-1-propenyl)- → HCID 70620984, compound

https://huagongshe.com/reaction/1657783

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzene, (3-chloro-1-propenyl)-HCID 94242—
ReactantHCID 21388458HCID 21388458—
SolventBenzeneHCID 241—
ProductHCID 70620984HCID 70620984—

Reaction Steps

To 3.6 g. of N-(α-cyano-3,4-dimethoxybenzyl)piperazine was added 8 ml. of benzene and then 1.47 g. of soda ash. To the resulting mixture was added 2.53 g. of cinnamyl chloride over a period of about 1 hour while the mixture was heated under reflux with stirring. After dropping, the mixture was further refluxed with stirring for 2 hours. After cooling, the mixture was filtered and the filtrate was washed with water and dried over sodium sulfate. The solvent was distilled off under reduced pressure. To the residue was added ligroin to be allowed to stand to give crystal which was collected by filtration. The product was recrystallized from ligroin to give 3.4 g. of crystal having a melting point of 119° - 123°C. This crystal was dissolved in benzene and the resultant solution was saturated with dry hydrochloric gas to separate crystal which was collected by filtration. Recrystallization from methanol afforded N-(α-cyano-3,4-dimethoxybenzyl)-N'-cinnamyl piperazine dihydrochloride as needles melting at 203° - 204.6°C. (decomposition).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03962247
Source datasetuspto-grants-1976_06
ORD IDord-fea43e5d5f6749bba87cf8f5d6a0e67b
Source noteuspto-grants-1976_06