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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 569647Generated: October 25, 2026

p-Toluenesulfonic acid → Pyrrolidine, 1-(6-chloro-3,4-dihydro-2-naphthalenyl)-

https://huagongshe.com/reaction/569647

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantPyrrolidineHCID 31268—
Reactant6-Chloro-2-tetraloneHCID 4456139—
SolventTolueneHCID 1140—
ProductPyrrolidine, 1-(6-chloro-3,4-dihydro-2-naphthalenyl)-HCID 10444008—

Reaction Steps

1155 g (6.4 mol) of 6-chloro-3,4-dihydro-2(1H)-naphthalenone were dissolved in 5 l of toluene, 500 g (7.0 mol) of pyrrolidine and subsequently a solution of 26 g (0.14 mol) of p-toluenesulphonic acid in toluene were added dropwise thereto and the mixture was boiled under reflux. When about 120 ml of water had separated, 4 l of toluene were distilled off and the mixture was left to cool slowly. A solid crystallized out. Filtration and washing with acetone gave 1-(6-chloro-3,4-dihydro-2-naphthyl)pyrrolidine of melting point 117°-118°. Concentration of the mother liquor, suspension of the residue in ether, filtration and washing with acetone gave a further portion of the above product of melting point 117°-118°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04732979
Source datasetuspto-grants-1988_03
ORD IDord-8b2cd8d887db431cba9bbb09b872f1ba
Source noteuspto-grants-1988_03