HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → Ethyl 3-{2-(3-methoxypropoxy)-4'-[(4-methylpiperazin-1-yl)methyl]biphenyl-4-yl}propanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | 1-Methylpiperazine | HCID 53167 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | Ethyl 3-[4'-formyl-2-(3-methoxypropoxy)biphenyl-4-yl]propanoate | HCID 86633297 | — |
| Solvent | 1,1-Dichloroethane | HCID 6365 | — |
| Product | Ethyl 3-{2-(3-methoxypropoxy)-4'-[(4-methylpiperazin-1-yl)methyl]biphenyl-4-yl}propanoate | HCID 66906778 | 80% |
Reaction Steps
Ethyl 3-[4′-formyl-2-(3-methoxypropoxy)biphenyl-4-yl]propanoate (1 g, 2.7 mmol) was dissolved in dichloroethane (20 mL). At 0° C., acetic acid (0.02 mL, 0.4 mmol) was added, followed, by N-methylpiperazine (0.3 g, 3 mmol) and sodium triacetoxyborohydride (0.86 g, 4 mmol) portionwise. The mixture was stirred at room temperature overnight. At 0° C., saturated aqueous sodium bicarbonate was added. The aqueous layer was extracted three times with dichloromethane. The combined organic layers were washed with brine and water, dried over anhydrous sodium sulfate, filtered and evaporated under reduced pressure to yield 0.98 g (80%) of the desired product as a brown oil used in the following step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08153647B2 |
| Source dataset | uspto-grants-2012_04 |
| ORD ID | ord-59d8dbcf29a846b582255b24c6f48397 |
| Source note | uspto-grants-2012_04 |