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Hydrazine hydrate (1:1) → HCID 54417124, compound

HRID 2396904
Notes
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Reaction equation

HRID 2396904 reaction equation
[CH2:1]([C:3](=[CH:18][CH:19]([CH3:21])[CH3:20])[CH:4]=[CH:5][CH2:6][N:7]1C(=O)C2=CC=CC=C2C1=O)[CH3:2].O.NN>C(O)C>[CH2:1]([C:3](=[CH:18][CH:19]([CH3:20])[CH3:21])[CH:4]=[CH:5][CH2:6][NH2:7])[CH3:2]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 24654Hydrazine hydrate (1:1)HCID 54211318HCID 54211318, compound

Product 1

HCID 54417124HCID 54417124, compound

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent

Procedure

A mixture of N-(4-ethyl-6-methyl-2,4-heptadiene-1-yl)phthalimide (17.62 g), hydrazine monohydrate (9.9 g), and ethanol (700 ml) was refluxed for 90 minutes under nitrogen atmosphere. The reaction mixture was evaporated in vacuo. The residue was dissolved in 10% aqueous potassium carbonate solution and extracted with ethyl acetate. The organic extract was washed with brine, dried over anhydrous magnesium sulfate, and evaporated to give 4-ethyl-6-methyl-2,4-heptadiene-1-ylamine as an oil.

Workup

  1. temperaturewas refluxed for 90 minutes under nitrogen atmosphere
  2. customThe reaction mixture was evaporated in vacuo
  3. dissolutionThe residue was dissolved in 10% aqueous potassium carbonate solution
  4. extractionextracted with ethyl acetate
  5. extractionThe organic extract
  6. washwas washed with brine
  7. dry with materialdried over anhydrous magnesium sulfate
  8. customevaporated

Sources & evidence

ORD record
ord-20db761e03f74cfb808683b698074923
Source dataset
uspto-grants-1996_02
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US05495023

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes