HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1660485Generated: November 1, 2026
p-Toluenesulfonic acid → HCID 20556815, compound
https://huagongshe.com/reaction/1660485
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | 2-Mepp | HCID 91965 | — |
| Reactant | HCID 14915831 | HCID 14915831 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 20556815 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04308266 |
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| Source dataset | uspto-grants-1981_12 |
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| ORD ID | ord-d5ec2635def34477ae3a903ae1166128 |
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| Source note | uspto-grants-1981_12 |
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