Hydrogen Peroxide → HCID 20389946, compound

HRID 426777Notes

Reaction equation

HRID 426777 reaction equation
[O:1]=[C:2]1[C:6]([CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][C:13]([OH:15])=[O:14])=[CH:5][CH2:4][CH2:3]1.[OH:16]O.[OH-].[Na+]>CO>[O:1]1[CH:2]2[CH2:3][CH2:4][C:5](=[O:16])[C:6]12[CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][C:13]([OH:15])=[O:14]

Participants

5

Procedure

A stirred solution of 7-(5-oxocyclopent-1-enyl)heptanoic acid (16.5 g) in methanol (400 ml) was treated slowly with aqueous hydrogen peroxide solution (32 ml; 100 volume strength) and 4N sodium hydroxide solution (28 ml) at 5° to 10° C. and allowed to stand at room temperature for 18 hours. The solution was concentrated in vacuo (to a volume of about 100 ml) and water (100 ml) was then added to the residue. The mixture was washed with chloroform and the chloroform discarded. The aqueous solution was then acidified to pH 3 by means of glacial acetic acid. The mixture was extracted with chloroform and the chloroform extract was washed with water and dried over magnesium sulphate. The solvent was removed in vacuo to give (±)-7-(1,2-epoxy-5-oxocyclopentyl)heptanoic acid (16.0 g), pure enough for use in the preparation of (±)-7-(4-acetoxy-5-oxocyclopent-1-enyl)heptanoic acid without further purification.

Workup

  1. concentrationThe solution was concentrated in vacuo (to a volume of about 100 ml) and water (100 ml)
  2. additionwas then added to the residue
  3. washThe mixture was washed with chloroform
  4. extractionThe mixture was extracted with chloroform
  5. extractionthe chloroform extract
  6. washwas washed with water
  7. dry with materialdried over magnesium sulphate
  8. customThe solvent was removed in vacuo

Sources & evidence

ORD record
ord-b13920c36f0c448d99fb55c4fdef2f0a
Source dataset
uspto-grants-1979_10
Patent number
US04171375

Reaction notes

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