Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1690615Generated: November 1, 2026

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

https://huagongshe.com/reaction/1690615

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant1-AcetylpiperazineHCID 83795—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantEthyl 3-[4'-formyl-2-(3-methoxypropoxy)biphenyl-4-yl]propanoateHCID 86633297—
Solvent1,1-DichloroethaneHCID 6365—
ProductEthyl 3-{4'-[(4-acetylpiperazin-1-yl)methyl]-2-(3-methoxypropoxy)biphenyl-4-yl}propanoateHCID 6690668578.3%

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-acetylpiperazine (0.38 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 1.02 g (78%) of the desired product as a brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08153647B2
Source datasetuspto-grants-2012_04
ORD IDord-31f732a759514b65a74654383207441d
Source noteuspto-grants-2012_04