1-Benzyl-4-piperidone → HCID 21918910, compound

HRID 278859Notes

Reaction equation

HRID 278859 reaction equation
[H-].[Na+].[CH2:3](P([O-])(=O)[O-])[P:4]([O:9][CH2:10][CH3:11])(=[O:8])[O:5][CH2:6][CH3:7].C([N:23]1[CH2:28][CH2:27][C:26](=O)[CH2:25][CH2:24]1)C1C=CC=CC=1>O1CCCC1>[NH:23]1[CH2:28][CH2:27][CH:26]([CH2:3][P:4](=[O:8])([O:9][CH2:10][CH3:11])[O:5][CH2:6][CH3:7])[CH2:25][CH2:24]1

Participants

5

Procedure

2.11 g (528 mmol) of 60% strength sodium hydride are initially charged in 50 ml of absolute tetrahydrofuran, and 15.7 g (52.8 mmol) of diethyl methanediphosphonate are added dropwise. The mixture is stirred at room temperature for another 30 minutes, and 10.1 g (52.8 mmol) of 1-benzyl-4-piperidone are then added. The mixture is stirred for one hour at room temperature and for one hour under reflux, concentrated, admixed with water and extracted three times with dichloromethane, and the organic phases are dried over sodium sulphate and concentrated. The residue is hydrogenated in 50 ml of ethanol over 1.7 g of 10% palladium-carbon at room temperature and 3 bar. The catalyst is filtered off with suction and the filtrate is concentrated.

Workup

  1. stirringThe mixture is stirred for one hour at room temperature and for one hour
  2. temperatureunder reflux
  3. concentrationconcentrated
  4. extractionextracted three times with dichloromethane
  5. dry with materialthe organic phases are dried over sodium sulphate
  6. concentrationconcentrated
  7. customis hydrogenated in 50 ml of ethanol over 1.7 g of 10% palladium-carbon at room temperature
  8. filtrationThe catalyst is filtered off with suction
  9. concentrationthe filtrate is concentrated

Sources & evidence

ORD record
ord-748ef14ca4e249b0ab144761123fbcef
Source dataset
uspto-grants-2002_03
Patent number
US06362178B1

Reaction notes

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