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ChemicalBook CAS DataBase List β-Estradiol
50-28-2

β-Estradiol synthesis

14synthesis methods
Estradiol, estra-1,3,5(10)-trien-3,17β-diol (28.1.17), is most easily made by reducing the keto-group of estrone by various reducing agents, in particular potassium borohydride.

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Yield:50-28-2 78%

Reaction Conditions:

with proton-exchanged montmorillonite in dichloromethane at 20;

Steps:

4.12. General procedure for H-mont-mediated deprotectionof PMB-protected ethers 23a-h

General procedure: To a solution of p-methoxybenzyl ether (0.366 mmol) in anhydrousCH2Cl2 (3 mL) was added H-mont (260 mg). Thereaction mixture was stirred at room temperature until theTLC indicated the consumption of the starting material. Themixture was filtered to remove H-mont. The filtrate was evaporatedunder reduced pressure. The residue was purified by flashchromatography (petroleum ether/ethyl acetate 20:1 to 1:1) togive the product. Following the procedure, 24a-h were prepared.

References:

Chen, Dongyin;Xu, Chang;Deng, Jie;Jiang, Chunhuan;Wen, Xiaoan;Kong, Lingyi;Zhang, Ji;Sun, Hongbin [Tetrahedron,2014,vol. 70,# 11,p. 1975 - 1983]

β-Estradiol Related Search:

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