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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 481980Generated: October 30, 2026

Iodine → 1-Methyl-4-(2-(4-acetamidophenoxy)acetyl)piperidine

https://huagongshe.com/reaction/481980

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
Reactant4-chloro-N-methylpiperidineHCID 79342—
ReactantMagnesiumHCID 5462224—
ReactantN-methyl-N-methoxy 2-(4-acetamidophenoxy)acetamideHCID 19064553—
Catalyst1,1-DibromoethaneHCID 11201—
SolventTetrahydrofuranHCID 8028—
Product1-Methyl-4-(2-(4-acetamidophenoxy)acetyl)piperidineHCID 1906457647%

Reaction Conditions

Temperature0 °C

Reaction Steps

A crystal of iodine was added to 0.45 gm (18.7 mMol) magnesium turnings covered with 6 mL tetrahydrofuran. To this mixture were added 5-6 drops of dibromoethane and the mixture was heated with a heat gun to initiate the reaction. Once the iodine color disappeared, 2 mL (15 mMol) 1-methyl-4-chloropiperidine were added and heating continued for an additional 30 seconds. After the exothermic reaction no longer maintained reflux temperature, the reaction mixture was heated at reflux for 30 minutes and was then cooled to 0° C. To the cold mixture was added the previously prepared N-methyl-N-methoxy 2-(4-acetamidophenoxy)acetamide and the resulting mixture stirred for 30 minutes at 0° C. and then an additional hour after warming to room temperature. The reaction was quenched by the addition of water and the resulting mixture extracted well with ethyl acetate. The combined organic extracts were washed saturated aqueous ammonium chloride, dried over magnesium sulfate, and concentrated under reduced pressure. The resulting residue was subjected to silica gel chromatography, eluting with dichloromethane containing 5% methanol. Fractions shown to contain product were combined and concentrated under reduced pressure to provide 0.90 gm (47%) of the desired ketone.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05792763
Source datasetuspto-grants-1998_08
ORD IDord-e1ff3663367d447fbbd9479ae00b1b43
Source noteuspto-grants-1998_08