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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1820290Generated: October 26, 2026

Acetic Acid → N-[2-[1-[2-[4-(p-Toluidino)piperidin-1-yl]ethyl]cyclohexyl]ethyl]phthalimide

https://huagongshe.com/reaction/1820290

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantN-(4-Methylphenyl)-4-piperidinamineHCID 23020914—
ReactantN-[2-[1-(formylmethyl)cyclohexyl]ethyl]phthalimideHCID 23109901—
Solvent1,2-DichloroethaneHCID 11—
ProductN-[2-[1-[2-[4-(p-Toluidino)piperidin-1-yl]ethyl]cyclohexyl]ethyl]phthalimideHCID 23109896108.4%

Reaction Steps

After adding sodium triacetoxyborohydride (0.82 g, 3.85 mmol) to a solution of 4-(p-toluidino)piperidine (0.73 g, 3.85 mmol), N-[2-[1-(formylmethyl)cyclohexyl]ethyl]phthalimide (0.77 g, 2.57 mmol) and acetic acid (0.30 mL, 5.14 mmol) in 1,2-dichloroethane (10 mL), the mixture was stirred at room temperature for 1.5 hours. Saturated aqueous sodium hydrogencarbonate was then added, and extraction was performed with chloroform-ethanol (10:1). After drying (anhydrous sodium sulfate), the solvent was distilled off under reduced pressure. The obtained residue was purified by silica gel column chromatography (25 g Merck Art 9385, chloroform:methanol=20:1) to obtain the title compound as a colorless oil (1.32 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07601843B2
Source datasetuspto-grants-2009_10
ORD IDord-72a61791c9db43b5bf9b16751be1ca19
Source noteuspto-grants-2009_10