Hydrochloric Acid → HCID 15284546, compound

HRID 1081699Notes

Reaction equation

HRID 1081699 reaction equation
[CH3:1][C:2]1([CH3:20])[C:6]2(OCC[O:7]2)[CH2:5][N:4]([C@@H:11]([C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)[CH3:12])[C:3]1=[O:19].Cl.C1(C)C=CC(S(O)(=O)=O)=CC=1>CC(C)=O>[CH3:20][C:2]1([CH3:1])[C:6](=[O:7])[CH2:5][N:4]([C@@H:11]([C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)[CH3:12])[C:3]1=[O:19]

Participants

5

Procedure

A mixture of 18.23 g of 9,9-dimethyl-8-oxo-7-[1-(R)-phenylethyl]-7-aza-1,4-dioxaspiro[4.4]nonane, 70 ml of 1N hydrochloric acid and 20 g of p-toluenesulfonic acid in 250 ml of acetone was heated under reflux for 20 hrs. During the reaction, 20 g of p-toluenesulfonic acid was further added. Solvent was removed under reduced pressure and the residue was extracted with chloroform. The extract was washed with a saturated sodium bicarbonate aqueous solution and dried. Solvent was removed under reduced pressure, and the residue was purified by silica gel chromatography (300 g of silica gel in a column) while eluting with a mixture of n-hexane and ethyl acetate (4:1, v/v) to yield 11.85 g of the titled compound.

Workup

  1. temperaturewas heated
  2. temperatureunder reflux for 20 hrs
  3. additionwas further added
  4. customSolvent was removed under reduced pressure
  5. extractionthe residue was extracted with chloroform
  6. washThe extract was washed with a saturated sodium bicarbonate aqueous solution
  7. customdried
  8. customSolvent was removed under reduced pressure
  9. customthe residue was purified by silica gel chromatography (300 g of silica gel in a column)
  10. washwhile eluting with a mixture of n-hexane and ethyl acetate (4:1

Sources & evidence

ORD record
ord-d1873e8467554551a23c58066b067c9e
Source dataset
uspto-grants-1996_12
Patent number
US05587386

Reaction notes

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