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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1457736Generated: October 30, 2026

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

https://huagongshe.com/reaction/1457736

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantAcetic AnhydrideHCID 7918—
Reactant2-DimethylaminopyridineHCID 21885—
ReactantDiisopropyl 4-hydroxy-4-phenyl-1,3-butanedicarboxylateHCID 19364502—
SolventPyridineHCID 1049—
ProductDiisopropyl 4-acetoxy-4-phenyl-1,3-butanedicarboxylateHCID 19364488—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05849747
Source datasetuspto-grants-1998_12
ORD IDord-0ed6ad94c3b14bae833d74be40ed831a
Source noteuspto-grants-1998_12