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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2406234Generated: November 2, 2026

4-Piperidone → HCID 67054566, compound

https://huagongshe.com/reaction/2406234

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-PiperidoneHCID 33721—
ReactantDiisopropylethylamineHCID 81531—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant2-(4-chlorophenyl)-5,5-dimethyl-1-Cyclohexene-1-carboxaldehydeHCID 44594330—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 67054566HCID 6705456640%

Reaction Steps

A suspension of the hydrochloride salt of 4-oxopiperidine (273 mg, 2.01 mmol) and DIPEA (351 μL, 2.01 mmol) was stirred in DCE (9.0 mL) at room temperature for 10 minutes. 2-(4-Chlorophenyl)-5,5-dimethylcyclohex-1-enecarbaldehyde (500 mg, 2.01 mmol) was then added, followed by NaBH(OAc)3 (426 mg, 2.01 mmol) and activated molecular sieves (˜1 g). The resulting suspension was stirred at room temperature for 16 hours. The reaction mixture was then filtered through a plug of Celite, rinsing with EtOAc. The filtrate was washed sequentially with saturated aqueous NaHCO3, water, and brine. The organic layer was dried over MgSO4 and concentrated. The crude residue was purified by flash chromatography on silica gel to afford the title compound (262 mg, 40% yield). MS (ESI) m/e (M+H+): 331.88

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08809352B2
Source datasetuspto-grants-2014_08
ORD IDord-abb07a5dd35b4d7e9229bb558a9a620c
Source noteuspto-grants-2014_08