Ethanol → HCID 20310097, compound

HRID 1606745Notes

Reaction equation

HRID 1606745 reaction equation
S(=O)(=O)(O)O.[C:6]([C:14]1[CH:22]=[CH:21][CH:20]=[C:19]2[C:15]=1[CH2:16][CH2:17][CH:18]2[C:23]([OH:25])=[O:24])(=[O:13])[C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1.[CH2:26](O)[CH3:27]>>[C:6]([C:14]1[CH:22]=[CH:21][CH:20]=[C:19]2[C:15]=1[CH2:16][CH2:17][CH:18]2[C:23]([O:25][CH2:26][CH3:27])=[O:24])(=[O:13])[C:7]1[CH:8]=[CH:9][CH:10]=[CH:11][CH:12]=1

Participants

4

Procedure

To 250 ml. of ethanol is added 20 ml. of concentrated sulfuric acid, followed by the addition of 13.3 g. of 4-benzoylindan-1-carboxylic acid. The mixture is refluxed for 5.5 hours. After cooling, the ethanol is distilled off under reduced pressure and water is added to the residue, followed by extraction with ether. The ethereal layer is washed with a 5 % aqueous solution of sodium hydroxide and a saturated aqueous solution of sodium chloride and, then, dried. The solvent is distilled off under reduced pressure and the residue is purified by column chromatography on silica gel (eluted with chloroform). The described procedure gives ethyl 4-benzoylindan-1-carboxylate as an oily product.

Workup

  1. temperatureThe mixture is refluxed for 5.5 hours
  2. temperatureAfter cooling
  3. distillationthe ethanol is distilled off under reduced pressure and water
  4. additionis added to the residue
  5. extractionfollowed by extraction with ether
  6. washThe ethereal layer is washed with a 5 % aqueous solution of sodium hydroxide
  7. dry with materiala saturated aqueous solution of sodium chloride and, then, dried
  8. distillationThe solvent is distilled off under reduced pressure
  9. customthe residue is purified by column chromatography on silica gel (eluted with chloroform)

Sources & evidence

ORD record
ord-9d93e7be10df4fc9a3121d0a5f4f09ac
Source dataset
uspto-grants-1976_04
Patent number
US03953500

Reaction notes

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