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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 854517Generated: October 30, 2026

4-(Trifluoromethyl)benzoic acid → Sodium 4-(trifluoromethyl)benzoate

https://huagongshe.com/reaction/854517

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Trifluoromethyl)benzoic acidHCID 9966—
ReactantSodium HydroxideHCID 14798—
SolventMethanolHCID 887—
ProductSodium 4-(trifluoromethyl)benzoateHCID 23717385—

Reaction Steps

To a solution of 4-trifluoromethyl benzoic acid (0.100 g, 0.239 mmole) in methanol (2.0 mL), is added sodium hydroxide (0.093 g, 0.287 mmole) and stirred at room temperature for 2 hours. The mixture is concentrated to dryness in vacuo to give sodium 4-trifluoromethyl-benzoate as a white solid. It is then mixed with NH4OAc (8.32 g, 107.9 mmole) in glacial acetic acid (500 mL) and heated at 100° C. for 16 hours. After removed the solvents on rota-vapor, the residue is partitioned between ethyl acetate (300 mL) and saturated sodium bicarbonate (300 mL). Extracted the aqueous layer with ethyl acetate (300 mL) one more time. The combined organic is ish with brine (3×500 mL), dried over Na2SO4, filtered and concentrated. The crude product is purified by chromatography on silica gel column, gradient elute with 0 to 10% ethyl acetate in hexane and concentrated to provide the titled compound as a white solid. Mass [EI+] 300 (M++H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07259175B2
Source datasetuspto-grants-2007_08
ORD IDord-fd9a1b8e0efc4f61ab1a0c87c6f3e84b
Source noteuspto-grants-2007_08