Hydrochloric Acid → HCID 56609273, compound

HRID 1789622Notes

Reaction equation

HRID 1789622 reaction equation
OO.[CH2:3]([CH:11]1[C:15](=[CH:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][C:22]([O:24][CH3:25])=[O:23])[C:14](=[O:26])[CH:13]=[CH:12]1)[CH:4]=[CH:5][CH2:6][CH2:7][CH2:8][CH2:9][CH3:10].[OH-].[Na+].[Cl-:29].[NH4+].Cl.C(=O)([O-])O.[Na+]>CO.CC(C)=O>[Cl:29][C:13]1[C:14](=[O:26])[C:15](=[CH:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][C:22]([O:24][CH3:25])=[O:23])[CH:11]([CH2:3][CH:4]=[CH:5][CH2:6][CH2:7][CH2:8][CH2:9][CH3:10])[CH:12]=1

Participants

9

Reactant 6

HCID 313Hydrochloric AcidHCID 784Hydrogen PeroxideHCID 14798Sodium HydroxideHCID 25517Ammonium ChlorideHCID 516892Sodium BicarbonateHCID 56625554HCID 56625554, compound

Product 1

HCID 56609273HCID 56609273, compoundYield 54%

Reagents, catalysts & solvents 2

HCID 180AcetoneSolventHCID 887MethanolSolvent

Procedure

0.3 ml of 30% aqueous hydrogen peroxide was added to a solution of 75 mg (226 micromol) of 4-(2-octenyl)-5-(6-methoxycarbonylhexylidene)-2-cyclopentenone in 3 ml of methanol under ice cooling and stirring, and then 70 microliters of 1N sodium hydroxide was added. The mixture was stirred at 0° C. for 20 minutes. A saturated aqueous solution of ammonium chloride was added, and the mixture was extracted with hexane. The organic layer was washed with a saturated aqueous solution of sodium chloride and dried over anhydrous sodium sulfate. The dried product was filtered and concentrated to give an oily product. The product was dissolved in 3 ml of acetone, and 0.5 ml of concentrated hydrochloric acid was added. The mixture was stirred for one hour. A saturated aqueous solution of sodium hydrogen carbonate was added, and the mixture was extracted with ethylacetate. The organic layer was washed with a saturated aqueous solution of sodium chloride and dried over anhydrous sodium sulfate. The dried product was filtered, concentrated and subjected to silica gel column chromatography (silica gel, 10 g; eluent, cyclohexane:ethylacetate=10:1) to give 45 mg (yield 54%) of 2-chloro-4-(2-octenyl)-5-(6-methoxycarbonylhexylidene)-2-cyclopentenone.

Workup

  1. stirringThe mixture was stirred at 0° C. for 20 minutes
  2. extractionthe mixture was extracted with hexane
  3. washThe organic layer was washed with a saturated aqueous solution of sodium chloride
  4. dry with materialdried over anhydrous sodium sulfate
  5. filtrationThe dried product was filtered
  6. concentrationconcentrated
  7. customto give an oily product
  8. stirringThe mixture was stirred for one hour
  9. extractionthe mixture was extracted with ethylacetate
  10. washThe organic layer was washed with a saturated aqueous solution of sodium chloride
  11. dry with materialdried over anhydrous sodium sulfate
  12. filtrationThe dried product was filtered
  13. concentrationconcentrated

Sources & evidence

ORD record
ord-98581098cec54663807316b620000b2c
Source dataset
uspto-grants-1987_08
Patent number
US04689426

Reaction notes

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