Reaction #2161

ord-fa7780e37be9447bbaf8e57cbcbe5c93

Reaction equation

CC(C(=O)O)C(=O)c1ccc(Cl)cc1
4-chlorobenzoylpropionic acid
CC(=O)[O-].[Na+]
sodium acetate
CC(C)(C)NN.Cl
t-butylhydrazine hydrochloride
CC(C)(C)N1N=C(c2ccc(Cl)cc2)CCC1=O
expected product
Yield 34.4%
CC(C)(C)N1N=C(c2ccc(Cl)cc2)CCC1=O
6-(4-chlorophenyl)-4,5-dihydro-2-t-butylpyridazinone
Yield 34.4%

Solvents

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    TemperatureThe resulting mixture was refluxed for 9 hours
  2. 2
    workup.DISTILLATIONdistilling off 65 ml of n-butanol during that time
  3. 3
    TemperatureThe resulting mixture was cooled
  4. 4
    workup.ADDITIONpoured into water (500 ml)
  5. 5
    Extractionextracted with methylene chloride (3×150 ml)
  6. 6
    WashThe combined organic layers were washed with 2% aqueous sodium hydroxide (3×100 ml), water (2×100 ml), 2% aqueous hydrochloric acid (3×100 ml), and water (1×100 ml)
  7. 7
    Otherdried
  8. 8
    Otherevaporated under vacuum

Procedure

To a solution of 4-chlorobenzoylpropionic acid (4.24 g) in n-butanol (150 ml) was added anhydrous sodium acetate (1.54 g) and t-butylhydrazine hydrochloride (2.75 g) portionwise at room temperature. The resulting mixture was refluxed for 9 hours distilling off 65 ml of n-butanol during that time. The resulting mixture was cooled and poured into water (500 ml) and extracted with methylene chloride (3×150 ml). The combined organic layers were washed with 2% aqueous sodium hydroxide (3×100 ml), water (2×100 ml), 2% aqueous hydrochloric acid (3×100 ml), and water (1×100 ml), dried and evaporated under vacuum yielding 1.71 g of the expected product.

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05728694uspto-grants-1998_03