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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1875314Generated: October 26, 2026

Ethyl bromoacetate → 2-((8-(Trifluoromethyl)quinolin-4-yl)oxy)acetic acid

https://huagongshe.com/reaction/1875314

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantPotassium CarbonateHCID 11430—
ReactantSodium HydroxideHCID 14798—
Reactant8-(Trifluoromethyl)quinolin-4-olHCID 178516442—
SolventDimethyl SulfoxideHCID 679—
Product2-((8-(Trifluoromethyl)quinolin-4-yl)oxy)acetic acidHCID 53420975—

Reaction Steps

4-Hydroxy-8-trifluoromethylquinoline (0.50 g, 2.35 mmol) was dissolved in DMSO (2 mL). Potassium carbonate was added (0.32 g, 2.35 mmol) and the mixture was stirred vigorously for 2 h. Ethyl bromoacetate (0.32 mL, 1.2 equiv) was added dropwise and heat was applied at 50° C. for 6 h. At 50° C., 2N NaOH (2 mL) was added and stirring continued for 4 h. The mixture was cooled and quenched with water (4 mL). Glacial acetic acid (1.4 mL) was added to ˜pH 4 resulting in precipitation of product. After stirring the suspension for 6 h, the solid was collected by vacuum filtration, rinsed with water, and dried in a vacuum dessicator over CaCl. The yield of white solid was 0.56 g (87%). 1H-NMR (DMSO-d6) 5.04 (s, 2H), 7.11 (d, J=5.2 Hz, 1H), 7.69 (t, J=8.0 Hz, 1H), 8.15 (d, J=8.0 Hz, 1H), 8.47 (d, J=8.0 Hz, 1H), 8.83 (d, J=5.2 Hz, 1H), 13.3 (br s, 1H); LC/MS (10-99%) M/Z: obs=333.5; tR=2.63 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08309543B2
Source datasetuspto-grants-2012_11
ORD IDord-c3c767114cdb4b15afac4c1d71efe410
Source noteuspto-grants-2012_11