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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1485484Generated: October 30, 2026

Ingenol → (4S,5R,6R,18R)-4,5-dihydroxy-3,8,8,15,15,18-hexamethyl-7,9-dioxapentacyclo[11.5.1.01,5.06,11.014,16]nonadeca-2,11-dien-19-one

https://huagongshe.com/reaction/1485484

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIngenolHCID 442042—
ReactantSodium BicarbonateHCID 516892—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
SolventAcetoneHCID 180—
Product(4S,5R,6R,18R)-4,5-dihydroxy-3,8,8,15,15,18-hexamethyl-7,9-dioxapentacyclo[11.5.1.01,5.06,11.014,16]nonadeca-2,11-dien-19-oneHCID 9182774569%

Reaction Steps

Ingenol (1.00 g, 2.30 mmol) was dissolved in a solution of p-toluenesulphonic acid monohydrate in acetone (0.47 mg/mL, 22.5 mL). The solution was stirred at room temperature for 25 min. To this solution was added a saturated aqueous solution of NaHCO3 (0.2 mL). The obtained mixture was concentrated in vacuo. The residue was taken up in brine and extracted with ethyl acetate. The combined organic phases were dried over sodium sulfate and concentrated in vacuo. The residue was purified by flash chromatography (heptane/ethyl acetate 19:1 heptane/ethyl acetate 0:1), giving the title compound as a white solid (616 mg, 69%). (See also: Opferkuch, H. J. et. al., Z. Naturforsch., (1981), 86b, 878-887.)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09422309B2
Source datasetuspto-grants-2016_08
ORD IDord-37f5dfc2229846f3a6b45d2b9a1f7547
Source noteuspto-grants-2016_08