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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1404776Generated: October 30, 2026

Hydrochloric Acid → 2-(5,7-Difluoroquinolin-6-yl)acetic acid

https://huagongshe.com/reaction/1404776

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSulfuric AcidHCID 1118—
ReactantNitrobenzeneHCID 7416—
ReactantSodium HydroxideHCID 14798—
Reactant2-(4-Amino-2,6-difluorophenyl)acetic acidHCID 55253383—
SolventGlycerolHCID 753—
SolventMethanolHCID 887—
Product2-(5,7-Difluoroquinolin-6-yl)acetic acidHCID 57742335480.4%

Reaction Conditions

Temperature150 °C

Reaction Steps

A mixture of 4-amino-2,6-difluorophenylacetic acid (3.2 g, 17.1 mmol), ferrous sulphate (1.04 g, 3.76 mmol), nitrobenzene (1.05 ml, 10.26 mmol) and conc. H2SO4 in glycerol (5.2 ml) was heated at 150° C. for 16 h. The mixture was cooled to RT, methanol (28 ml) was added followed by aq. 6N NaOH (28 ml) and heated at 110° C. for 3 h. After cooling to RT, the mixture was acidified with conc. HCl to pH 3.0. The precipitate formed was filtered, washed with water and dried under vacuum. The precipitate was refluxed with methanol, filtered under hot conditions and the filtrate was evaporated to give the title compound 11 g, 25%) as a brown solid, 1H-NMR (δ ppm, DMSO-d6, 400 MHz): δ12.72 (bs, 1H), 8.98 (d, J=3.1 Hz, 1H): 8.47 (d, J=8.4, 1H); 7.71 (d, J=9.7, 1H); 7.62 (dd, J=8.4, 4.1, 2H); 3.85 (s, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08912331B2
Source datasetuspto-grants-2014_12
ORD IDord-48f356e5599b412190443986205652e4
Source noteuspto-grants-2014_12