HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 490704Generated: October 29, 2026
4-(Trifluoromethyl)benzoic acid → Sodium 4-(trifluoromethyl)benzoate
https://huagongshe.com/reaction/490704
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-(Trifluoromethyl)benzoic acid | HCID 9966 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Sodium 4-(trifluoromethyl)benzoate | HCID 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 wash 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07528160B2 |
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| Source dataset | uspto-grants-2009_05 |
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| ORD ID | ord-083583a5a03f439f881cb08b9283fbb8 |
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| Source note | uspto-grants-2009_05 |
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