HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 508019Generated: October 28, 2026
Acetic Acid → Methyl 3-(4-{[(2',6'-dimethylbiphenyl-3-yl)methyl]amino}phenyl)propanoate
https://huagongshe.com/reaction/508019
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Citric Acid | HCID 311 | — |
| Reactant | Methyl 3-(4-aminophenyl)propanoate | HCID 417374 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | 2',6'-Dimethylbiphenyl-3-carbaldehyde | HCID 23082866 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Methyl 3-(4-{[(2',6'-dimethylbiphenyl-3-yl)methyl]amino}phenyl)propanoate | HCID 23157312 | 61% |
Reaction Steps
To a solution of methyl 3-(4-aminophenyl)propanoate (3.33 g, 18.6 mmol) and 2′,6′-dimethylbiphenyl-3-carbaldehyde (3.91 g, 18.6 mmol) in toluene (40 mL) were added molecular sieves (0.4 nm, beads, 7.2 g), and the mixture was stirred at room temperature for 55 hr. The reaction mixture was filtered through celite, and the filtrate was concentrated under reduced pressure. The obtained residue was dissolved in tetrahydrofuran (100 mL). Sodium cyanoborohydride (2.53 g, 40.3 mmol) and acetic acid (2.31 mL, 40.3 mmol) were successively added, and the mixture was stirred under a nitrogen atmosphere at room temperature for 3 hr. Aqueous citric acid solution was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (10%-40% ethyl acetate/hexane) to give the title compound (4.24 g, yield 61%) 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-9b8b0fa50f304b4dbe34b1e4298862c7 |
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| Source note | uspto-grants-2010_08 |
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