Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1639934Generated: October 31, 2026

Trifluoroacetic acid → HCID 66720879, compound

https://huagongshe.com/reaction/1639934

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 66720882HCID 66720882—
SolventDichloromethaneHCID 6344—
ProductHCID 66720879HCID 6672087996.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

Add 1 mL (13 mmol) of trifluoroacetic acid to a solution of 700 mg (1.3 mmol) of methyl 5-(2-chloro-5-ethoxyphenyl)-6-{4-chloro-3-[(4-methoxybenzyl)oxy]phenyl}pyridine-2-carboxylate in 10 mL of DCM stirred at 0° C. Stir the reaction mixture for 2 h at 20° C. then concentrate under reduced pressure. Take up the residue in 50 mL of DCM and wash with 50 mL of a saturated aqueous solution of NaHCO3. Dry the organic phase over Na2SO4 and concentrate under reduced pressure. Purify the residue obtained by silica gel column chromatography, eluting with a cyclohexane/EtOAc gradient from 0 to 30% of EtOAc. After concentration under reduced pressure, we obtain 524 mg of methyl 5-(2-chloro-5-ethoxyphenyl)-6-(4-chloro-3-hydroxyphenyl)pyridine-2-carboxylate in the form of oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08110579B2
Source datasetuspto-grants-2012_02
ORD IDord-3c2da43b6d2143a2a09d5573f6386806
Source noteuspto-grants-2012_02