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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1690610Generated: October 31, 2026

Acetic Acid → Ethyl 3-{2-(3-methoxypropoxy)-4'-[(4-methylpiperazin-1-yl)methyl]biphenyl-4-yl}propanoate

https://huagongshe.com/reaction/1690610

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant1-MethylpiperazineHCID 53167—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantEthyl 3-[4'-formyl-2-(3-methoxypropoxy)biphenyl-4-yl]propanoateHCID 86633297—
Solvent1,1-DichloroethaneHCID 6365—
ProductEthyl 3-{2-(3-methoxypropoxy)-4'-[(4-methylpiperazin-1-yl)methyl]biphenyl-4-yl}propanoateHCID 6690677880%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08153647B2
Source datasetuspto-grants-2012_04
ORD IDord-59d8dbcf29a846b582255b24c6f48397
Source noteuspto-grants-2012_04