4068-92-2

Upstream product

• 152-58-9 C₂₁H₃₀O₄ 

Downstream Products

• 50-03-3 11β,17α,21-trihydroxypregn-4-ene-3,20-dione-21-acetate 
• 6818-44-6 4-((3R,5S,7R,10S,12S,13R)-3,7,12-Triacetoxy-10,13-dimethyl-hexadecahydro-cyclopenta[a]phenanthren-17-yl)-pentanoic acid methyl ester 
• 807-05-6 17α.20;20.21-Bis-methylendioxy-pregnen-(4)-ol-(11β)-on-(3); 'Bismethylendioxy-hydrocortison' 

Relevant academic research and scientific papers

Dehalogenation methodof 9-halogenated steroid compound and application

The invention provides a dehalogenation method of a 9-halogenated steroid compound and application, and relates to the technical field of chemical synthesis. The dehalogenation method of the 9-halogenated steroid compound comprises the following steps: reacting a compound I with a hydrogen donor and an azo radical initiator to obtain a 9-dehalogenated product compound II of the 9-halogenated steroid compound. According to the dehalogenation method of the 9-halogenated steroid compound, a hydrogen donor adopts one or a combination of more of hypophosphorous acid and hypophosphite, formic acid and formate, organic silicon hydride, hydrazine compounds or cyclohexene, and an initiator adopts an azo free radical initiator. Reagents such as chromium, divalent chromium salt, trivalent chromium salt or tributyltin hydride which are high in toxicity and cause serious pollution to the environment are not used in the reaction, the method is green and environmentally friendly, the synthesis process is simple, convenient and easy to implement, and the production applicability is improved.