Acetone → 6-Benzoyl-2,3-dihydro-1H-indene-1-carboxamide

HRID 1606742Notes

Reaction equation

HRID 1606742 reaction equation
CC(C)=[O:3].[CH2:5]([C:12]1[CH:20]=[C:19]2[C:15]([CH2:16][CH2:17][CH:18]2[C:21]([NH2:23])=[O:22])=[CH:14][CH:13]=1)[C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1.[Cr](O[Cr]([O-])(=O)=O)([O-])(=O)=O.[Na+].[Na+].S(=O)(=O)(O)O>O>[C:5]([C:12]1[CH:20]=[C:19]2[C:15]([CH2:16][CH2:17][CH:18]2[C:21]([NH2:23])=[O:22])=[CH:14][CH:13]=1)(=[O:3])[C:6]1[CH:7]=[CH:8][CH:9]=[CH:10][CH:11]=1

Participants

6

Procedure

To 150 ml. of acetone is added 12.5 g. of 6-benzylindan-1-carboxamide, followed by the dropwise addition of a solution of 5 g. of sodium dichromate in 24 ml. of 6N sulfuric acid. After the addition has been completed, the mixture is stirred overnight. Then, 200 ml. of water is added and the acetone is distilled off under reduced pressure. The residue is extracted with ethyl acetate. The extract is washed with water and dried, followed by removal of the solvent by distillation under reduced pressure. The residue is purified by column chromatography (500 g. of silica gel; eluted with a 7:3 solvent mixture of chloroform and acetone) and the resultant crude crystals are recrystallized from benzene. The procedure gives 6-benzoylindan-1-carboxamide as crystals melting at 195°-197°C.

Workup

  1. additionAfter the addition
  2. distillationthe acetone is distilled off under reduced pressure
  3. extractionThe residue is extracted with ethyl acetate
  4. washThe extract is washed with water
  5. customdried
  6. customfollowed by removal of the solvent by distillation under reduced pressure
  7. customThe residue is purified by column chromatography (500 g
  8. washeluted with a 7:3 solvent mixture of chloroform and acetone) and the resultant crude crystals
  9. customare recrystallized from benzene

Sources & evidence

ORD record
ord-bf0639361892432d95be2bee4c8c1d85
Source dataset
uspto-grants-1976_04
Patent number
US03953500

Reaction notes

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