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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1088811Generated: November 3, 2026

Sodium hydride → 8-(5-Methoxy-2-benzimidazolyl)thiomethyl-1-methyl-1,2,3,4-tetrahydroquinoline

https://huagongshe.com/reaction/1088811

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant1-Methyl-8-chloromethyl-1,2,3,4-tetrahydroquinoline hydrochlorideHCID 22161791—
ReactantHCID 178488032HCID 178488032—
Catalyst18-Crown-6HCID 28557—
SolventDimethylformamideHCID 6228—
Product8-(5-Methoxy-2-benzimidazolyl)thiomethyl-1-methyl-1,2,3,4-tetrahydroquinolineHCID 1505333249.7%

Reaction Steps

A solution of 5-methoxy-2-mercaptobenzimidazole(0.9 g), sodium hydride (60% in oil, 0.20 g) and 18-crown-6(i.e. 1,4,7,10,13,16-hexaoxacyclooctadecane) (50 mg) in dimethyl formamide (15 ml) was stirred for 20 minutes at room temperature. To the mixture was added a solution of 1-methyl-8-chloromethyl-1,2,3,4-tetrahydroquinoline hydrochloride (1.1 g) in dimethyl formamide (15 ml) and the solution was stirred for 20 hours at room temperature. Dimethyl formamide was distilled off, and chloroform, 30% aqueous solution of sodium hydroxide and water were added to the resulting residue. The mixture was stirred for 2 hours and extracted with chloroform. After drying over anhydrous magnesium sulfate, the solvent was distilled off. The resultant residue was purified by silica gel column chromatography [eluent:n-hexane-ethyl acetate (4:1)] to give 8-(5-methoxy-2-benzimidazolyl)thiomethyl-1-methyl-1,2,3,4-tetrahydroquinoline (0.80 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04963566
Source datasetuspto-grants-1990_10
ORD IDord-ec7016845283424a859cb5b6bb637fa4
Source noteuspto-grants-1990_10