Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 400766Generated: October 26, 2026

Sodium Hydroxide → 2'-Methyl-2-(trifluoromethyl)-[1,1'-biphenyl]-4-carboxylic acid

https://huagongshe.com/reaction/400766

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantMethyl 2'-methyl-2-(trifluoromethyl)-[1,1'-biphenyl]-4-carboxylateHCID 58554190—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product2'-Methyl-2-(trifluoromethyl)-[1,1'-biphenyl]-4-carboxylic acidHCID 59495813—

Reaction Conditions

Temperature60 °C

Reaction Steps

A solution of methyl 2′-methyl-2-(trifluoromethyl)biphenyl-4-carboxylate (5 g; 16.99 mmol; 1 eq.) in EtOH (150 mL) at RT was treated with sodium hydroxide (10.2 mL; 5 M; 51 mmol; 3 eq.). The reaction mixture was stirred at 60° C. for 2 hours. The reaction mixture was concentrated to give a brown solid which was taken up in water (300 mL) and the aqueous phase was washed twice with EtOAc. The aqueous phase was acidified with HCl cc to pH 2, then it was concentrated until precipitation (half of the volume). The suspension was filtered affording the title compound as a beige solid. 1H NMR (DMSO-d6, 300 MHz) δ 13.55 (br s, 1H), 8.31 (s, 1H), 8.26-8.23 (d, J=7.90 Hz, 1H), 7.51-7.48 (d, J=7.90 Hz 1H), 7.37-7.12 (m, 4H), 1.99 (s, 3H). LC/MS (Method A): 278.9 (M−H)−. HPLC (Method A) Rt 4.57 min (Purity: 98.7%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08741923B2
Source datasetuspto-grants-2014_06
ORD IDord-152486e92ea840989240212ef511088e
Source noteuspto-grants-2014_06