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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1660485Generated: November 1, 2026

p-Toluenesulfonic acid → HCID 20556815, compound

https://huagongshe.com/reaction/1660485

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
Reactant2-MeppHCID 91965—
ReactantHCID 14915831HCID 14915831—
SolventTolueneHCID 1140—
ProductHCID 20556815HCID 20556815—

Reaction Steps

6 g of methoxy-2-tetralone together with 6 g of N-(o-tolyl)-piperazine are dissolved in 100 ml of toluene whilst warming, 300 mg of p-toluenesulphonic acid are added and the solution refluxed for 24 hours, whereby the water is separated using a Dean-Stark separator. The reaction mixture is then evaporated to dryness, 200 ml of dimethyl formamide and 300 mg of a 10% palladium on charcoal catalyst are added to the obtained 3,4-dihydro-6-methoxy-2-[4-(2-methylphenyl)-1-piperazinyl]-naphthalene, which is hydrogenated at normal pressure. When the take-up of hydrogen ceases the catalyst is filtered off, the solvent evaporated off and the residue chromatographed on Kieselgel with methylene chloride (methanol (99:1). The title compound is obtained as a compact residue. M.P. 286-288° [Hydrochloride salt form].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04308266
Source datasetuspto-grants-1981_12
ORD IDord-d5ec2635def34477ae3a903ae1166128
Source noteuspto-grants-1981_12