HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 508034Generated: November 1, 2026
4'-(2-Ethoxyethoxy)-2',6'-dimethylbiphenyl-3-carbaldehyde → Ethyl 3-[4-({[4'-(2-ethoxyethoxy)-2',6'-dimethylbiphenyl-3-yl]methyl}amino)-2-fluorophenyl]propanoate
https://huagongshe.com/reaction/508034
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4'-(2-Ethoxyethoxy)-2',6'-dimethylbiphenyl-3-carbaldehyde | HCID 23111722 | — |
| Reactant | Ethyl 3-(4-amino-2-fluorophenyl)propanoate | HCID 23157234 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Ethyl 3-[4-({[4'-(2-ethoxyethoxy)-2',6'-dimethylbiphenyl-3-yl]methyl}amino)-2-fluorophenyl]propanoate | HCID 23157676 | 83.4% |
Reaction Steps
To a solution of ethyl 3-(4-amino-2-fluorophenyl)propanoate (1.48 g, 7.00 mmol) and 4′-(2-ethoxyethoxy)-2′,6′-dimethylbiphenyl-3-carbaldehyde (2.09 g, 7.00 mmol) in toluene (15 mL) were added molecular sieves (0.4 nm, beads, 3.5 g), and the mixture was stirred at room temperature for 30 hr. The reaction mixture was filtered through celite, and the filtrate was concentrated under reduced pressure. The obtained residue was dissolved in ethanol (20 mL), 10% palladium-carbon (50% water-containing product, 0.5 g) was added, and the mixture was stirred under a hydrogen atmosphere (balloon pressure) at room temperature for 12 hr. The catalyst was filtered off, and the obtained filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (5%-30% ethyl acetate/hexane) to give the title compound (2.88 g, yield 83%) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07786165B2 |
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| Source dataset | uspto-grants-2010_08 |
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| ORD ID | ord-9dd6a26878ed4ca7983b691c719db763 |
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| Source note | uspto-grants-2010_08 |
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