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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1869153Generated: October 25, 2026

Lithium hydroxide, monohydrate → 1-(2-(Trifluoromethyl)quinolin-4-yl)-1H-indole-3-carboxylic acid

https://huagongshe.com/reaction/1869153

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium hydroxide, monohydrateHCID 168937—
Reactant3-methoxycarbonyl-1-(2-(trifluoromethyl)quinol-4-yl)-1H-indoleHCID 68970592—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product1-(2-(Trifluoromethyl)quinolin-4-yl)-1H-indole-3-carboxylic acidHCID 68972955—

Reaction Steps

0.204 g (4.9 mmol) of lithium hydroxide monohydrate and 8 cm3 of water are added to 0.6 g (1.62 mmol) of 3-methoxycarbonyl-1-(2-(trifluoromethyl)quinol-4-yl)-1H-indole dissolved in 8 cm3 of tetrahydrofuran. After stirring at reflux for 15 hours, the reaction mixture is concentrated to dryness under reduced pressure (2.7 kPa) to give a residue which is taken up in 20 cm3 of water (pH=10). The resulting aqueous solution is washed with 30 cm3 of ethyl acetate, adjusted to pH 6 with N hydrochloric acid and extracted with 50 cm3 of ethyl acetate. The organic phase is dried over magnesium sulphate and concentrated to dryness under reduced pressure (2.7 kPa). The solid obtained is triturated in 20 cm3 of isopropyl ether and filtered off, resulting in 0.3 g of 3-carboxy-1-(2-(trifluoromethyl)quinol-4-yl)-1H-indole in the form of a yellow powder. Mass spectrum (EI): m/e 356 (M+•), m/e 311.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07638521B2
Source datasetuspto-grants-2009_12
ORD IDord-d37b4a9f20ea4fc38641b5986370be79
Source noteuspto-grants-2009_12