Aniline → HCID 178468312, compound

HRID 2089734Notes

Reaction equation

HRID 2089734 reaction equation
[NH2:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[N:8]([O-])=O.[Na+].C([O-])(=O)C.[Na+].[C:17]([CH2:20][C:21](=[O:23])[CH3:22])(=[O:19])[CH3:18]>C(O)(=O)C.Cl.O.C(O)C>[C:2]1([NH:1][N:8]=[C:20]([C:21](=[O:23])[CH3:22])[C:17](=[O:19])[CH3:18])[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1

Participants

9

Conditions

Temperature
0 °C

Procedure

To a solution of aniline (2000 mg, 21.50 mmol) in 30 mL of acetic acid and 5 mL of concentrated hydrochloride solution, sodium nitrite (1780 mg, 25.80 mmol) in 8 mL of water was added dropwise at 0° C., and the mixture was stirred at 0° C. for 1 h. Then to the reaction mixture was added dropwise a solution of sodium acetate (5290 mg, 64.50 mmol) and acetylacetone (2795 mg, 27.95 mmol) in 20 mL of ethanol and 12 mL of water. The mixture was stirred at room temperature overnight, filtered, washed with water, EtOH/H2O (1:1) and hexane, and dried to give 3-(phenylhydrazono)pentane-2,4-dione (2955 mg, 67%).

Workup

  1. stirringThe mixture was stirred at room temperature overnight
  2. filtrationfiltered
  3. washwashed with water, EtOH/H2O (1:1) and hexane
  4. customdried

Sources & evidence

ORD record
ord-b9020364ae3946bd9c5c01069f012843
Source dataset
uspto-grants-2013_05
Patent number
US08435995B2

Reaction notes

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