Reaction #446435

ord-365598da8dfa4a518c5c99307f72946e

Reaction equation

[Na+].[OH-]
sodium hydroxide
O=S(=O)([O-])OOS(=O)(=O)[O-].[NH4+].[NH4+]
ammonium peroxodisulfate
COC(=O)c1cncn1C1c2ccccc2CC1(C)C
1-(2,2-dimethylindan-1-yl)-5-imidazolecarboxylic acid methyl ester
O=S(=O)(O)O
sulfuric acid
COC(=O)c1cncn1C1c2ccccc2C(=O)C1(C)C
1-(2,2-dimethyl-3-oxoindan-1-yl)-5-imidazolecarboxylic acid methyl ester
Yield 60.2%

Solvents

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    Temperatureis heated to +80° C
  2. 2
    Temperaturethe solution is cooled to +7° C.
  3. 3
    ExtractionThe solution is extracted twice
  4. 4
    Dryingthe organic phase is dried over sodium sulfate
  5. 5
    Concentrationconcentrated to dryness by evaporation
  6. 6
    workup.ADDITIONis added
  7. 7
    FiltrationThe resulting suspension is filtered
  8. 8
    Concentrationthe filtrate is concentrated by evaporation
  9. 9
    Otherthe residue is crystallised from an ether/hexane mixture

Procedure

A mixture of 30.0 g of 1-(2,2-dimethylindan-1-yl)-5-imidazolecarboxylic acid methyl ester, 150 ml of water and 17 g of sulfuric acid is heated to +80° C. Within a period of 1.5 hours a solution of 114 g of ammonium peroxodisulfate is added dropwise thereto. When the reaction is complete, the solution is cooled to +7° C. and adjusted to pH 3 by the addition of 30% sodium hydroxide solution. The solution is extracted twice using 200 ml of methylene chloride each time, and the organic phase is dried over sodium sulfate and concentrated to dryness by evaporation. The residue is taken up in a small amount of methylene chloride, and ether is added. The resulting suspension is filtered, the filtrate is concentrated by evaporation and the residue is crystallised from an ether/hexane mixture. 19 g of 1-(2,2-dimethyl-3-oxoindan-1-yl)-5-imidazolecarboxylic acid methyl ester having a melting point of 104°-108° C. are obtained.

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05000777uspto-grants-1991_03