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

HRID 1244220Notes

Reaction equation

HRID 1244220 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-714ca6ce941642dfad6aeab1b6220dd1
Source dataset
uspto-grants-2006_10
Patent number
US07122540B2

Reaction notes

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