Hydrochloric Acid → Diisopropyl 4-acetoxy-4-phenyl-1,3-butanedicarboxylate

HRID 1457736Notes

Reaction equation

HRID 1457736 reaction equation
CN(C1C=CC=CN=1)C.[OH:10][CH:11]([C:27]1[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=1)[CH:12]([C:21]([O:23][CH:24]([CH3:26])[CH3:25])=[O:22])[CH2:13][CH2:14][C:15]([O:17][CH:18]([CH3:20])[CH3:19])=[O:16].[C:33](OC(=O)C)(=[O:35])[CH3:34].Cl>N1C=CC=CC=1>[C:33]([O:10][CH:11]([C:27]1[CH:28]=[CH:29][CH:30]=[CH:31][CH:32]=1)[CH:12]([C:21]([O:23][CH:24]([CH3:26])[CH3:25])=[O:22])[CH2:13][CH2:14][C:15]([O:17][CH:18]([CH3:19])[CH3:20])=[O:16])(=[O:35])[CH3:34]

Participants

6

Reactant 4

HCID 313Hydrochloric AcidHCID 7918Acetic AnhydrideHCID 218852-DimethylaminopyridineHCID 19364502Diisopropyl 4-hydroxy-4-phenyl-1,3-butanedicarboxylate

Product 1

HCID 19364488Diisopropyl 4-acetoxy-4-phenyl-1,3-butanedicarboxylate

Reagents, catalysts & solvents 1

HCID 1049PyridineSolvent

Procedure

70 mg of dimethylaminopyridine was added to a mixed solution comprising 6.13 g of diisopropyl 4-hydroxy-4-phenyl-1,3-butanedicarboxylate, 30 ml of pyridine and 6 ml of acetic anhydride, followed by stirring at room temperature for 1.5 hours. 2N hydrochloric acid was added to the reaction solution, and then the mixture was extracted with ethyl acetate. The organic layer was sequentially washed with 2N hydrochloric acid, a saturated sodium hydrogencarbonate aqueous solution and a saturated sodium chloride aqueous solution and dried over anhydrous magnesium sulfate. The drying agent was filtered off, and then, the solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate=5/1) to obtain 4.68 g of the above-identified compound as a colorless oily substance.

Workup

  1. extractionthe mixture was extracted with ethyl acetate
  2. washThe organic layer was sequentially washed with 2N hydrochloric acid
  3. dry with materiala saturated sodium hydrogencarbonate aqueous solution and a saturated sodium chloride aqueous solution and dried over anhydrous magnesium sulfate
  4. filtrationThe drying agent was filtered off
  5. distillationthe solvent was distilled off under reduced pressure
  6. customThe residue was purified by silica gel column chromatography (hexane/ethyl acetate=5/1)

Sources & evidence

ORD record
ord-0ed6ad94c3b14bae833d74be40ed831a
Source dataset
uspto-grants-1998_12
Patent number
US05849747

Reaction notes

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