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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 596486Generated: October 30, 2026

Phosphorus sulfide (P2S5) → 8-Cyano-3-methyl-5,6,7,8-tetrahydroquinoline

https://huagongshe.com/reaction/596486

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus sulfide (P2S5)HCID 14817—
Reactant3-Methyl-5,6,7,8-tetrahydroquinoline-8-carboxamideHCID 12278227—
SolventPyridineHCID 1049—
Product8-Cyano-3-methyl-5,6,7,8-tetrahydroquinolineHCID 1227821052.2%

Reaction Steps

3-Methyl-5,6,7,8-tetrahydroquinoline-8-carboxamide (3.6 g.) in pyridine (54 ml.) was treated with P2S5 (7.56 g.) and the mixtures heated at reflux with stirring for 3 hours. The solvent was removed under reduced pressure and the residue cooled in ice-water then made basic with 10% NaOH. The basic solution was extracted with chloroform (3 times) and the combined extracts extracted with 2NHCl (twice). The combined acid extracts were basified with solid sodium carbonate and extracted into chloroform (3 times). The combined chloroform extracts were washed with brine dried (MgSO4) and evaporated to give the title compound 1.7 g. This was converted to the hydrochloride by dissolving in ether and adding ethereal HCl. An oily residue was formed from which the supernatent liquid was decanted. The residue was triturated twice with dry ether and the remaining solid recrystallised from isopropyl alcohol giving the hydrochloride of the title compound m.p. 189° C. Analysis Found: C, 63.08; H, 6.26; N, 13.34% C11H12N 2 HCl requires: C, 63.30; H, 6.28; N, 13.43%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04011225
Source datasetuspto-grants-1977_03
ORD IDord-219432f22e6d45faadc1e3c0b594718a
Source noteuspto-grants-1977_03