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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1079235Generated: November 1, 2026

Toluene → HCID 54228505, compound

https://huagongshe.com/reaction/1079235

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
Reactant2-ChloroquinolineHCID 11928—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 22865068HCID 22865068—
CatalystTetrabutylammonium ChlorideHCID 70681—
SolventWaterHCID 962—
ProductHCID 54228505HCID 5422850511.4%

Reaction Steps

A 50 mL round bottom flask was charged with (+)-(4aR)-(10bR)-4-methyl-8-hydroxy-10b-methyl-1,2,3,4,4a,-5,6,10b-octahydrobenzo[f]quinolin-3-one (300 mg, 1.22 mmol), tetrabutylammonium chloride (339 mg, 1.22 mmol), 2-chloroquinoline (200 mg, 1.22 mmol), 4 mL of 50% sodium hydroxide solution, and 4 mL of toluene, fitted with a reflux condenser, and the stirred mixture was heated at 100°, under nitrogen, for 24 h. The mixture was cooled, diluted with water (50 mL) and extracted with chloroform (3×100 mL). The combined organic extracts were dried over sodium sulfate, concentrated, and purified by silica gel chromatography (60% ethyl acetate/hexanes eluent; followed by an additional chromatography on a short silica column, eluting with 10% ethyl acetate/dichloromethane) to give 52 mg (11%) of the title compound as a white solid. mp 172°-174°. FDMS: m/e=372. α[D]589 =+67.74 (c=0.43, chloroform).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05550134
Source datasetuspto-grants-1996_08
ORD IDord-e2e452b69768485c982e38b7d775289a
Source noteuspto-grants-1996_08