Acetic Acid → HCID 22139884, compound

HRID 1847378Notes

Reaction equation

HRID 1847378 reaction equation
[OH-].[Na+].Cl.[N+:4]([C:7]1[CH:8]=[C:9]([NH:13][NH2:14])[CH:10]=[CH:11][CH:12]=1)([O-:6])=[O:5].C(O)(=O)C.[CH:19](=O)[CH2:20][CH3:21]>C(O)C>[N+:4]([C:7]1[CH:8]=[C:9]([NH:13]/[N:14]=[CH:19]/[CH2:20][CH3:21])[CH:10]=[CH:11][CH:12]=1)([O-:6])=[O:5]

Participants

6

Reactant 4

HCID 176Acetic AcidHCID 527PropanalHCID 14798Sodium HydroxideHCID 54642853-Nitrophenylhydrazinium(1+) chloride

Product 1

HCID 22139884HCID 22139884, compound

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent

Procedure

Sodium hydroxide solution (10%, 15 mL) was added slowly to a stirred suspension of (3-nitrophenyl)hydrazine hydrochloride (1.89 g, 10 mmol) in ethanol (20 mL) until pH 6. Acetic acid (5 mL) was added to the mixture followed by propionaldehyde (0.7 g, 12 mmol). After stirring for 3 h at room temperature, the mixture was poured into ice-water and the resulting precipitate was isolated by filtration, washed with water and dried in air to obtain (E)-1-(3-nitrophenyl)-2-propylidenehydrazine, which was used directly in the next step.

Workup

  1. customthe resulting precipitate was isolated by filtration
  2. washwashed with water
  3. customdried in air

Sources & evidence

ORD record
ord-5718385c245a4e058abd5dc161cf9e57
Source dataset
uspto-grants-2015_02
Patent number
US08952050B2

Reaction notes

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