Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1269617Generated: November 1, 2026

Acetic Acid → Ethyl [2-methyl-4-({[4'-(trifluoromethyl)-1,1'-biphenyl-3-yl]amino}methyl)phenoxy]acetate

https://huagongshe.com/reaction/1269617

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant4'-(Trifluoromethyl)-[1,1'-biphenyl]-3-amineHCID 2782708—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantEthyl (4-formyl-2-methylphenoxy)acetateHCID 58622891—
SolventDichloromethaneHCID 6344—
ProductEthyl [2-methyl-4-({[4'-(trifluoromethyl)-1,1'-biphenyl-3-yl]amino}methyl)phenoxy]acetateHCID 5862290285.7%

Reaction Steps

To a solution of ethyl (4-formyl-2-methylphenoxy)acetate (0.2 g, 0.9 mmol) in anhydrous CH2Cl2 (8 mL) was added 4′-(trifluoromethyl)-1,1′-biphenyl-3-ylamine (0.214 g, 0.9 mmol). The resulting mixture was stirred under nitrogen at room temperature for 15 mins, prior to addition of sodium triacetoxyborohydride (0.267 g, 1.26 mmol) and acetic acid (0.052 mL, 0.9 mmol). The resultant mixture was stirred for 18 h prior to quenching by cautious addition of sat. sodium bicarbonate solution (20 mL) the reaction mixture was then extracted CH2Cl2 (20 mL). The organic extract separated by hydrophobic frit and the solvent removed in vacuo. Purification by Biotage™ chromatography (Silica, 40 g) eluting 9:1 cyclohexane:EtOAc afforded the title compound as a colourless oil (0.342 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07199239B2
Source datasetuspto-grants-2007_04
ORD IDord-4c6068d9093c47a6a4fe3a221c55ad1d
Source noteuspto-grants-2007_04