Sulfuric Acid → Ethyl 2-[2-(3,5-dichlorophenyl)hydrazinylidene]propanoate

HRID 440386

Reaction equation

HRID 440386 reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]([NH:9][NH2:10])[CH:5]=[C:6]([Cl:8])[CH:7]=1.[C:11]([O:16][CH2:17][CH3:18])(=[O:15])[C:12]([CH3:14])=O.S(=O)(=O)(O)O.C(=O)(O)[O-].[Na+]>O.C(OCC)(=O)C.C(O)C>[Cl:1][C:2]1[CH:3]=[C:4]([NH:9][N:10]=[C:12]([CH3:14])[C:11]([O:16][CH2:17][CH3:18])=[O:15])[CH:5]=[C:6]([Cl:8])[CH:7]=1

Participants

8

Reactant 4

HCID 1118Sulfuric AcidHCID 12041Ethyl pyruvateHCID 516892Sodium BicarbonateHCID 6004693,5-Dichlorophenylhydrazine

Product 1

HCID 71333082Ethyl 2-[2-(3,5-dichlorophenyl)hydrazinylidene]propanoate

Reagents, catalysts & solvents 3

HCID 702EthanolSolventHCID 962WaterSolventHCID 8857Ethyl AcetateSolvent

Procedure

Combine 3,5-dichlorophenylhydrazine (300 g) and ethanol (2 L). Add ethyl pyruvate (153.6 mL) and sulfuric acid (25 mL). After 3 hours, evaporate in vacuo to obtain a residue. Cover the residue with ethyl acetate and water. Add solid sodium bicarbonate until the aqueous layer is neutralized. Separate the layers and extract the aqueous layer with ethyl acetate. Combine the organic layers, dry over MgSO4, filter, and evaporate in vacuo to give ethyl pyruvate-3,5-dichlorophenylhydrazone.

Workup

  1. customevaporate in vacuo
  2. customto obtain a residue
  3. customSeparate the layers
  4. extractionextract the aqueous layer with ethyl acetate
  5. dry with materialdry over MgSO4
  6. filtrationfilter
  7. customevaporate in vacuo

Sources & evidence

ORD record
ord-ce8140f302344c27b81a28d9e0b9b7d7
Source dataset
uspto-grants-1996_05
Patent number
US05519048

Linked notes

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