Sulfuric Acid → 2-(2'-Chlorophenyl)-1,3-cyclohexanedione

HRID 46792Notes

Reaction equation

HRID 46792 reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[CH2:8][C:9](=[O:16])[CH2:10][CH2:11][CH2:12][C:13](O)=[O:14].S(=O)(=O)(O)O>>[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[CH:8]1[C:9](=[O:16])[CH2:10][CH2:11][CH2:12][C:13]1=[O:14]

Participants

3

Reactant 2

HCID 1118Sulfuric AcidHCID 15595129HCID 15595129, compound

Product 1

HCID 128765992-(2'-Chlorophenyl)-1,3-cyclohexanedioneYield 63.2%

Conditions

Temperature
120 °C

Procedure

A 500 ml one-neck round bottom flask was charged with 10.0 g (0.0416 mol) of 6-(2'-chlorophenyl)-5-ketohexanoic acid and 100 ml of 72% sulfuric acid. The reaction mixture was stirred and heated to 120° C. for 5 1/2 hrs. (oil bath) then poured into 600 ml of ice water. A tacky, white solid formed, and this was extracted into 300 ml of methylene chloride. The CH2Cl2 solution was washed six times with water, dried over anhydrous MgSO4, and stripped to leave 8.87 g of a tacky, white solid. This material was recrystallized from ethyl acetate to give 5.85 g (63%) of 2-(2'-Chlorophenyl)-1,3-cyclohexanedione as a white, crystalline solid, m.p. 148.5°-149° C.

Workup

  1. customA tacky, white solid formed
  2. extractionthis was extracted into 300 ml of methylene chloride
  3. washThe CH2Cl2 solution was washed six times with water
  4. dry with materialdried over anhydrous MgSO4
  5. customto leave 8.87 g of a tacky, white solid
  6. customThis material was recrystallized from ethyl acetate

Sources & evidence

ORD record
ord-691b0b9716c046ec994e6763a876a8b9
Source dataset
uspto-grants-1979_11
Patent number
US04175135

Reaction notes

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