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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1056008Generated: October 25, 2026

Aniline → 2-(Phenylamino)quinoline-8-carboxylic acid

https://huagongshe.com/reaction/1056008

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnilineHCID 6115—
ReactantSodium hydrideHCID 24758—
Reactant2-Chloroquinoline-8-carboxylic acidHCID 19026201—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Product2-(Phenylamino)quinoline-8-carboxylic acidHCID 8978202335%

Reaction Conditions

Temperature50 °C

Reaction Steps

NaH (60% w/w in mineral oil; 0.549 g, 13.73 mmol) was added to a mixture of 2-chloroquinoline-8-carboxylic acid (181a, 0.95 g, 4.58 mmol) and aniline (0.834 ml, 9.15 mmol) in THF (11 ml) at 0° C.; the reaction was heated to 50° C. for 2 h. The mixture was diluted with 75 ml of Et2O and washed with 1 N NaOH. The organic layer was separated, and the aq. layer was acidified to ˜pH 1 with 5 N HCl and extracted 4 times with 75 ml of EtOAc. All organic extracts were then combined dried over Na2SO4, and concentrated to give 2-(phenylamino)quinoline-8-carboxylic acid (35% yield) as a light-brown solid. MS (ESI, pos. ion) m/z: 265.2 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09394297B2
Source datasetuspto-grants-2016_07
ORD IDord-c3d25280e6ad4f8382b91b7634928dcd
Source noteuspto-grants-2016_07