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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 28342Generated: October 25, 2026

Aluminum isopropoxide → 3-Hydroxy-2-iodo-estra-1,3,5(10)-triene-7,17-dione

https://huagongshe.com/reaction/28342

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAluminum isopropoxideHCID 11143—
Reactant3,7beta-Dihydroxy-2-iodo-estra-1,3,5(10)-trien-17-oneHCID 11611293—
SolventTolueneHCID 1140—
SolventCyclohexanoneHCID 7967—
Product3-Hydroxy-2-iodo-estra-1,3,5(10)-triene-7,17-dioneHCID 1168298363%

Reaction Steps

A solution of 206 mg (0.5 mmol) of 3,7β-dihydroxy-2-iodo-estra-1,3,5(10)-trien-17-one 14 in 15 ml of toluene and 4 ml of cyclohexanone was heated to 140° C. (oil bath temperature), and a solution of 400 mg of aluminum isopropylate in 10 ml of toluene was added drop by drop. In the meantime, a portion of the reaction mixture was distilled off. After complete addition of the aluminum isopropylate, it was refluxed for still another 5 hours. Then, the reaction solution was cooled and diluted with 80 ml of dichloromethane and 30 ml of potassium/sodium tartrate solution, and the resulting mixture was first stirred vigorously for 30 minutes before the organic phase was separated from the aqueous phase. The aqueous phase was finally extracted with dichloromethane (3×30 ml), and the combined organic phases were washed with a saturated NaCl solution, dried on sodium sulfate and concentrated by evaporation in a rotary evaporator. Flash chromatography (cyclohexane/ethyl acetate) yielded 129 mg (63%) of colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07419972B2
Source datasetuspto-grants-2008_09
ORD IDord-ba0076bd14184a21bb44fc4c93e651f8
Source noteuspto-grants-2008_09