Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1974024Generated: November 1, 2026

Hydrochloric Acid → 5,6,7,8-Tetrahydro-3-methyl-8-quinolinecarbothioamide

https://huagongshe.com/reaction/1974024

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantIsothiocyanatotrimethylsilaneHCID 75297—
Reactant3-Methyl-5,6,7,8-tetrahydroquinolineHCID 120028—
ReactantHCID 178418365HCID 178418365—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Product5,6,7,8-Tetrahydro-3-methyl-8-quinolinecarbothioamideHCID 30039215%

Reaction Steps

3-Methyl-5,6,7,8-tetrahydroquinoline (7.3g, 0.05 mol.) was added to a solution of isopropylmagnesium bromide [prepared from isopropylbromide (6.15g, 0.05 mol), magnesium (1.44g, 0.06 mol) in ether (10 ml.)] and the solution heated at 60° to remove the ether by distillation. Toluene (5 ml.) was added and the reaction mixture was heated at 120° for 2 hours, cooled, diluted with toluene (30 ml) and this solution was added to a solution of trimethylsilyl isothiocyanate (7.85 g, 0.06 mol) in toluene (50 ml.) at 0° C. The reaction mixture was stirred at room temperature for 12 hours, diluted with water (15 ml.) and the pH adjusted to 2.0 with Conc. HCl. The aqueous solution was extracted with ether and the extracts discarded. The aqueous solution was adjusted to pH 9.0 with Na2CO3 and extracted with chloroform (3 × 50 ml.). The combined extracts were washed with brine, dried and the solvent removed to give a mixture of 3-methyl-5,6,7,8-tetrahydroquinoline and the title compound (5%) which was isolated by chromatography and identified by comparison with authentic material.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04000142
Source datasetuspto-grants-1976_12
ORD IDord-c65e54a06ddb4d0ea2d89f82cd1787a7
Source noteuspto-grants-1976_12