HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → Methyl 4-((3-((phenylamino)methyl)phenoxy)methyl)benzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Aniline | HCID 6115 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | Methyl 4-((3-formylphenoxy)methyl)benzoate | HCID 28825911 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl 4-((3-((phenylamino)methyl)phenoxy)methyl)benzoate | HCID 86720705 | 64% |
Reaction Steps
To a stirred solution of methyl 4-((3-formylphenoxy)methyl)benzoate (464 mg, 1.72 mmol) in anhydrous DCM (8 mL) was added aniline (0.63 mL, 6.87 mmol) followed by glacial acetic acid (0.46 mL, 6.87 mmol). The reaction was stirred at room temperature for 18 hours. Sodium triacetoxyborohydride (1.52 g, 6.87 mmol) was added and the reaction was stirred at room temperature for 2 hours. The mixture was diluted with DCM (100 mL). The organic layer was washed with 1 N HCl (3×30 mL) and saturated aqueous NaHCO3 (30 mL) and passed through a hydrophobic fit. The solvent was removed in vacuo to afford the title compound as an oil that solidifies on standing (380 mg, 64% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09326976B2 |
| Source dataset | uspto-grants-2016_05 |
| ORD ID | ord-6b3f667027144974be333e5c74f978dc |
| Source note | uspto-grants-2016_05 |