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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1004950Generated: October 30, 2026

1-Benzyl-4-piperidone → 4-(2H-1,3-Benzodioxol-5-yl)-1-benzylpiperidin-4-ol

https://huagongshe.com/reaction/1004950

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Benzyl-4-piperidoneHCID 19220—
ReactantAmmonium ChlorideHCID 25517—
Reactant1-Bromo-3,4-(methylenedioxy)benzeneHCID 75831—
ReactantMagnesiumHCID 5462224—
SolventTetrahydrofuranHCID 8028—
Product4-(2H-1,3-Benzodioxol-5-yl)-1-benzylpiperidin-4-olHCID 22128034—

Reaction Conditions

Temperature50 °C

Reaction Steps

To 1.46 g of magnesium shavings, which had previously been covered with tetrahydrofuran, was added dropwise a solution of 12.06 g (60 mmol) of 5-bromo-benzo[1,3]dioxol in 30 ml of absolute tetrahydrofuran, followed by 11.35 g (60 mmol) of 1-benzyl-4-piperidone. The reaction mixture was stirred at 50° C. for 1 hour, then poured on to ice and ammonium chloride solution. The 4-benzo[1,3]dioxol-5-yl-1-benzyl-piperidin-4-ol formed was extracted with ethyl acetate and crystallized upon concentration of the solution. There were obtained 10.85 g (58% of theory) of white crystals; m.p.: 144° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06051712
Source datasetuspto-grants-2000_04
ORD IDord-481309fe81474a30be03ed5589a8b2b5
Source noteuspto-grants-2000_04