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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 54233Generated: October 26, 2026

1,2-Dichloroethane → Quinoline

https://huagongshe.com/reaction/54233

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantQuinaldic AcidHCID 7124—
Reactant1-HydroxybenzotriazoleHCID 75771—
SolventDimethylformamideHCID 6228—
ProductQuinolineHCID 7047319.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

A 100 ml RBF equipped with magnetic stir bar and N2 inlet was charged with 356 mg (2.06 mmol, 1 eq) 2-quinaldic acid in 10 ml dry DMF. The solution was cooled to 0° C. and 415 mg (3.07 mmol, 1.5 eq) HOBt was added followed by 415 mg EDC (2.16 mmol, 1.05 eq). The reaction was stirred 2 hours at 0° C. when 1.1 g (2.06 mmol, 1 eq) of free asparagine amine in 10 ml dry DMF was added. The reaction was stirred at 0° C. for 2 hours then room temperature overnight. The reaction was poured into sat. bicarb and extracted with 2×65 mL ethyl acetate. The combined organics were washed with 5% aq. citric acid, brine, dried and concentrated to 1.4 g crude foam. Purification by flash chromatography on silica gel (100% ethyl acetate) yielded 850 mg (61%) of quinoline adduct.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05622949
Source datasetuspto-grants-1997_04
ORD IDord-aa6c28ca5ebe489993550699923c7862
Source noteuspto-grants-1997_04