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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2093716Generated: October 31, 2026

Lithium Hydroxide → 2-(Methoxymethyl)-4-methyl-7-(trifluoromethyl)quinoline-3-carboxylic acid

https://huagongshe.com/reaction/2093716

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium HydroxideHCID 3939—
Reactant2-(Methoxymethyl)-4-methyl-7-(trifluoromethyl)quinoline-3-carboxylic acid methyl esterHCID 66584032—
SolventTetrahydrofuranHCID 8028—
Product2-(Methoxymethyl)-4-methyl-7-(trifluoromethyl)quinoline-3-carboxylic acidHCID 6658411466%

Reaction Conditions

Temperature60 °C

Reaction Steps

A 2M aq. LiOH sol. (9.3 ml) was added to a solution of 980 mg (3.1 mmol) 2-(methoxymethyl)-4-methyl-7-(trifluoromethyl)quinoline-3-carboxylic acid methyl ester in THF (25 ml) and the mixture was subsequently heated to 60° C. for 16 h. The THF was removed as far as possible in a vacuum and the obtained aqueous solution was washed with ether, the pH was set to 2 with 2M hydrochloric acid and dilution was performed with EtOAc. The organic phase was separated and washed with brine, dried over MgSO4 and concentrated in a vacuum. 612 mg (2.0 mmol, 66%) 2-(methoxymethyl)-4-methyl-7-(trifluoromethyl)quinoline-3-carboxylic acid was obtained as a residue. The raw product was further converted without additional purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08445512B2
Source datasetuspto-grants-2013_05
ORD IDord-e9aa2656e1464dd9ac8f7baa4755bfef
Source noteuspto-grants-2013_05