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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 6593Generated: October 25, 2026

2-Dimethylaminopyridine → 2',3'-Difluoro-4'-(4-pentyloxybutoxy)-biphenyl-4-carboxylic acid 4-[(R)-1-trifluoromethylheptyloxycarbonyl]-phenyl ester

https://huagongshe.com/reaction/6593

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-DimethylaminopyridineHCID 21885—
Reactant4-hydroxybenzoic acid (R)-1-trifluoromethyl-heptyl esterHCID 14549217—
Reactant4'-(4-Butoxybutoxy)-2',3'-difluorobiphenyl-4-carboxylic acidHCID 22016253—
SolventTetrahydrofuranHCID 8028—
SolventDiisopropylcarbodiimideHCID 12734—
Product2',3'-Difluoro-4'-(4-pentyloxybutoxy)-biphenyl-4-carboxylic acid 4-[(R)-1-trifluoromethylheptyloxycarbonyl]-phenyl esterHCID 5867963465%

Reaction Steps

To a solution of 4′-(4-butoxybutoxy)-2′,3′-difluorobiphenyl-4-carboxylic acid (27) (1 equi.), (4-hydroxybenzoic acid (R)-1-trifluoromethyl-heptyl ester (7) (1 equi.), and DMAP (dimethylaminopyridine) (0.1 equi.) in THF (25 mL/mmole), DIC (diisopropyl carbodiimide) (1.2 equi.) was added at room temperature. The reaction mixture was stirred at that temperature for 24 h, quenched with water, extracted with ethyl acetate:hexane(1:1), washed with brine, dried over MgSO4, and concentrated in vacuo. Purification by chromatography on silica gel (5% EtOAc/hexanes) gave 2′,3′-difluoro-4′-(4-pentyloxybutoxy)-biphenyl-4-carboxylic acid 4-[(R)-1-trifluoromethylheptyl oxycarbonyl]-phenyl ester (28) as a white solid (65%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07083832B2
Source datasetuspto-grants-2006_08
ORD IDord-a26dd92f0c2a4f80bcbf1d5d19358e72
Source noteuspto-grants-2006_08