Diethylamine → HCID 21333309, compound

HRID 1704723Notes

Reaction equation

HRID 1704723 reaction equation
C(CO[C:5](=[O:31])[C:6]1[CH:11]=[CH:10][C:9]([C:12]([C:25]2[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=2)([C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=2)[C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)=[CH:8][N:7]=1)#N.[CH2:32]([NH:34][CH2:35][CH3:36])[CH3:33]>O>[CH2:32]([N:34]([CH2:35][CH3:36])[C:5](=[O:31])[C:6]1[CH:11]=[CH:10][C:9]([C:12]([C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=2)([C:13]2[CH:14]=[CH:15][CH:16]=[CH:17][CH:18]=2)[C:25]2[CH:26]=[CH:27][CH:28]=[CH:29][CH:30]=2)=[CH:8][N:7]=1)[CH3:33]

Participants

4

Reactant 2

HCID 8021DiethylamineHCID 21333313HCID 21333313, compound

Product 1

HCID 21333309HCID 21333309, compound

Reagents, catalysts & solvents 1

HCID 962WaterSolvent

Procedure

Heat at reflux for 6 hours a mixture of 0.1 mole of cyanomethyl-5-(triphenylmethyl)-picolinate and 0.5 moles of diethylamine. Cool the reaction mixture, pour into water and extract with chloroform. Dry the chloroform layer over anhydrous sodium sulfate and evaporate to obtain thereby the product of this example.

Workup

  1. temperatureHeat
  2. temperatureat reflux for 6 hours
  3. temperatureCool the reaction mixture
  4. extractionextract with chloroform
  5. dry with materialDry the chloroform layer over anhydrous sodium sulfate
  6. customevaporate
  7. customto obtain

Sources & evidence

ORD record
ord-e5e8951469034936a6722fe135fcbadb
Source dataset
uspto-grants-1978_11
Patent number
US04127662

Reaction notes

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