Hydrochloric Acid → HCID 15284546, compound

HRID 378574Notes

Reaction equation

HRID 378574 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 a 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-d7209a94cf2c492aaeeb9df3fa52658b
Source dataset
uspto-grants-2000_02
Patent number
US06031102

Reaction notes

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