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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1107600Generated: October 30, 2026

Cyclohexanone → 12,14-Dihydroxy-3-oxocard-20(22)-enolide

https://huagongshe.com/reaction/1107600

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexanoneHCID 7967—
ReactantAluminum isopropoxideHCID 11143—
ReactantDigoxigeninHCID 15478—
SolventTolueneHCID 1140—
Product12,14-Dihydroxy-3-oxocard-20(22)-enolideHCID 20503189.5%

Reaction Steps

A mixture of 488 mg digoxigenin, 7.5 ml toluene, 3.75 ml cyclohexanone, and 550 mg aluminum isopropoxide was heated under reflux for 2.3 hours and then concentrated in vacuo to half of its original volume. Two hundred μl water was added and the mixture was evaporated in vacuo to dryness. The powdery solid was dried in vacuo over overnight. The dry residue was stirred in 25 ml methanol and the resulting mixture was filtered. The residue on the funnel was washed with 25 ml methanol. The filtrate and washing were combined and evaporated in vacuo affording 920 mg white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06060598
Source datasetuspto-grants-2000_05
ORD IDord-ba373593c86540c2b28bede3a478d518
Source noteuspto-grants-2000_05