Hydrochloric Acid → 1,4-Bis(phenylmethyl)piperazinone, hydrochloride

HRID 1413715Notes

Reaction equation

HRID 1413715 reaction equation
[CH2:1]([NH:8][CH2:9][CH2:10][NH:11][CH2:12][C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[Cl:19]CC([O:23][CH2:24][CH3:25])=O.C(=O)([O-])[O-].[Na+].[Na+].Cl>C(O)C.C(O)(C)C>[ClH:19].[C:13]1([CH2:12][N:11]2[CH2:10][CH2:9][N:8]([CH2:1][C:2]3[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=3)[CH2:25][C:24]2=[O:23])[CH:14]=[CH:15][CH:16]=[CH:17][CH:18]=1

Participants

7

Procedure

A mixture of N,N'-dibenzylethylenediamine (24.0 g., 0.1 mole), ethyl chloroacetate (V, 24.51 g., 0.2 mole), anhydrous sodium carbonate (10 g., 0.094 mole) in ethanol (250 ml.) is heated under reflux for 20 hours. The ethanol is removed under reduced pressure and the residue is partitioned between chloroform and water. Evaporation of the chloroform gives an oil which is dissolved in isopropanol (200 ml.) and acidified with ethereal hydrogen chloride. The precipitate of 1,4-bis(phenylmethyl)piperazinone hydrochloride is filtered off and recrystallized from isopropanol, m.p. 209°-212°.

Workup

  1. temperatureis heated
  2. temperatureunder reflux for 20 hours
  3. customThe ethanol is removed under reduced pressure
  4. customthe residue is partitioned between chloroform and water
  5. customEvaporation of the chloroform
  6. customgives an oil which
  7. filtrationThe precipitate of 1,4-bis(phenylmethyl)piperazinone hydrochloride is filtered off
  8. customrecrystallized from isopropanol, m.p. 209°-212°

Sources & evidence

ORD record
ord-36ec8d881bcd48b4bfc53b81d4428c8e
Source dataset
uspto-grants-1981_02
Patent number
US04251438

Reaction notes

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