Ethanol → HCID 20318957, compound

HRID 1605588Notes

Reaction equation

HRID 1605588 reaction equation
[NH2:1][C:2]1[C:13]([Br:14])=[CH:12][C:11]([C:15]#[N:16])=[CH:10][C:3]=1[CH2:4][N:5]([CH2:8][CH3:9])[CH2:6][CH3:7].C([OH:19])C.[OH-].[Na+]>O>[NH2:1][C:2]1[C:13]([Br:14])=[CH:12][C:11]([C:15](=[O:19])[NH2:16])=[CH:10][C:3]=1[CH2:4][N:5]([CH2:8][CH3:9])[CH2:6][CH3:7]

Participants

5

Reactant 3

HCID 702EthanolHCID 14798Sodium HydroxideHCID 20319049HCID 20319049, compound

Product 1

HCID 20318957HCID 20318957, compound

Reagents, catalysts & solvents 1

HCID 962WaterSolvent

Procedure

11 gm of 2-amino-3-bromo-5-cyano-N,N-diethyl-benzylamine were refluxed with a mixture of 70 ml of ethanol and 100 ml of 5 N sodium hydroxide. After cooling, the reaction solution was diluted with 100 ml of water and extracted with chloroform. The chloroform extract was dried over sodium sulfate and evaporated, and the residue was recrystallized from isopropanol, yielding 2-amino-3-bromo-5-carbamoyl-N,N-diethyl-benzylamine, m.p. 140°-142°C.

Workup

  1. temperatureAfter cooling
  2. extractionextracted with chloroform
  3. extractionThe chloroform extract
  4. dry with materialwas dried over sodium sulfate
  5. customevaporated
  6. customthe residue was recrystallized from isopropanol

Sources & evidence

ORD record
ord-8eee2a576f69408cb4a7d52231b59dc2
Source dataset
uspto-grants-1976_04
Patent number
US03950393

Reaction notes

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