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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 649181Generated: October 30, 2026

Sodium Hydroxide → 4-Allyloxy-8(2-benzimidazolyl)thio-3-methyl-5,6,7,8-tetrahydroquinoline

https://huagongshe.com/reaction/649181

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant2-ChlorobenzimidazoleHCID 78572—
ReactantThioureaHCID 2723790—
Reactant4-Allyloxy-8-bromo-3-methyl-5,6,7,8-tetrahydroquinolineHCID 14155523—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product4-Allyloxy-8(2-benzimidazolyl)thio-3-methyl-5,6,7,8-tetrahydroquinolineHCID 14155524—

Reaction Steps

0.46 Gram of 2-chlorobenzimidazole, 0.2 g of thiourea and 10 ml of ethanol were mixed together and the mixture was refluxed for 2 hours. To this reaction mixture was added 0.62 g of 4-allyloxy-8-bromo-3-methyl-5,6,7,8-tetrahydroquinoline and 0.3 g of sodium hydroxide, then the whole reaction mixture was refluxed for 5 hours. After the reaction was completed, ethanol was removed by evaporation, and to the residue thus obtained was added water and then extracted with chloroform, and the chloroform extract was dried with anhydrous magnesium sulfate, and the chloroform was removed by evaporation. The residue thus obtained was purified by means of a silica gel column chromatography (eluent: methylene chloride/methanol=100/1) to obtain 0.5 g of 4-allyloxy-8-(2-benzimidazolyl)thio-3-methyl-5,6,7,8-tetrahydroquinoline in the form of light brown oily substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04738970
Source datasetuspto-grants-1988_04
ORD IDord-738f98f2012b485b8a5241fbc8b2bf8c
Source noteuspto-grants-1988_04