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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1455839Generated: October 29, 2026

Pyridine → HCID 68954487, compound

https://huagongshe.com/reaction/1455839

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant4'-(Trifluoromethyl)(1,1'-biphenyl)-2-carboxylic acidHCID 55251—
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 69142509HCID 69142509—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductHCID 68954487HCID 68954487—

Reaction Steps

4′-Trifluoromethyl-2-biphenylcarboxylic acid was converted to the corresponding acid chloride by treatment with oxalyl chloride in methylene chloride in the presence of catalytic amount of DMF. To a solution of the acid chloride (10.8 g, 38 mmol) and pyridine (3.27 mL, 40 mmol) in methylene chloride (200 mL) was added the product of step (c) (10.1 g, 40 mmol), and the reaction mixture was stirred at room temperature for 1 hour. The reaction solution was diluted to 600 mL with CH2Cl2, washed with 0.1 N HCl solution (2×500 mL) and with brine (500 mL), and then dried (MgSO4). The solvent was evaporated in vacuo to give the crude product which was purified by recrystallization from EtOAc/isooctane to afford 13.8 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07482368B2
Source datasetuspto-grants-2009_01
ORD IDord-aebf058fb60a4cdd9351c61989bd274b
Source noteuspto-grants-2009_01