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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 579881Generated: November 3, 2026

p-Toluenesulfonic acid → HCID 22165459, compound

https://huagongshe.com/reaction/579881

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantAcrylamideHCID 6579—
ReactantPyrrolidineHCID 31268—
Reactant5-Chloro-2-TetraloneHCID 3562754—
SolventBenzeneHCID 241—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductHCID 22165459HCID 22165459—

Reaction Steps

11.07 g of 5-chloro-2-tetralone were boiled at reflux for 2 hours in 200 ml of benzene and 10.1 ml of pyrrolidine in the presence of 0.3 g of p-toluenesulphonic acid. The crude 1-(5-chloro-3,4-dihydro-2-naphthyl)pyrrolidine obtained was treated, without purification, with 9.0 g of acrylamide and 0.5 g of p-toluenesulphonic acid. The mixture was heated under nitrogen to 100° for 2 hours and to 150° for 2 hours. 250 ml of ethyl acetate and 50 ml of water were added to the reaction mixture, whereupon the insoluble constituents were filtered off, washed with ethyl acetate and water, dried and recrystallized from ethyl acetate. There was obtained 7-chloro-1,2,5,6-tetrahydrobenzo[f]quinolin-3(4H)-one of melting point 252°-253°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04749791
Source datasetuspto-grants-1988_06
ORD IDord-a8fa7a6d54614cbeb744bd60e337408f
Source noteuspto-grants-1988_06