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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | 4'-(Trifluoromethyl)-[1,1'-biphenyl]-3-amine | HCID 2782708 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | Ethyl (4-formyl-2-methylphenoxy)acetate | HCID 58622891 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Ethyl [2-methyl-4-({[4'-(trifluoromethyl)-1,1'-biphenyl-3-yl]amino}methyl)phenoxy]acetate | HCID 58622902 | 85.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07199239B2 |
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| Source dataset | uspto-grants-2007_04 |
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| ORD ID | ord-4c6068d9093c47a6a4fe3a221c55ad1d |
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| Source note | uspto-grants-2007_04 |
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