FIELD: chemistry.
SUBSTANCE: task is achieved by the disclosed method of producing 16α, 17α-cyclohex-3',4'-enopregn-5-en-3β-ol-20-one acetate by reacting 16-dehydropregnenolone acetate with 1,3-butadiene in the medium of an organic solvent in the presence of a Lewis acid, characterised by conducting the process in molar ratio 16-dehydropregnenolone acetate: 1,3-butadiene: Lewis acid equal to 1:2-3:0.2-0.4 at temperature of -10°C, and then raising temperature of the reaction mixture to room temperature, passing the reaction mixture through a sorbent layer and separating the end product using existing methods.
EFFECT: simple method of producing an intermediate product in synthesis of steroid hormones of the pregnane family by not conducting the process in a sealed apparatus.
3 cl, 6 ex
Title | Year | Author | Number |
---|---|---|---|
METHOD OF PRODUCING 16α,17α-CYCLOHEX-3',4'-ENOPREGN-5-EN-3β-OL-20-ONE ACETATE | 2011 |
|
RU2480476C1 |
METHOD OF PRODUCING 16α,17α-CYCLOHEXANO-5α,6α-EPOXYPREGN-3β-OL-20-ONE ACETATE | 2011 |
|
RU2480477C1 |
METHOD OF PRODUCING 6-METHYLENO-16α,17α-CYCLOHEXANOPREGN-4-ENE-3,20-DIONE | 2014 |
|
RU2566368C1 |
METHOD OF PRODUCING 16α, 17α-CYCLOHEXANOPREGN-5-EN-3β-OL-20-ONE ACETATE | 2012 |
|
RU2495047C1 |
METHOD OF PRODUCING 3β-ACETOXY-17α-HYDROPEROXY-16α-METHYLPREGNANES FROM Δ-20-KETOSTEROIDS AND METHOD OF PRODUCING 3β-ACETOXY-17α-HYDROXY-16α-METHYLPREGNANES USING 3β-ACETOXY-17α-HYDROPEROXY-16α-METHYLPREGNANES | 2009 |
|
RU2418805C1 |
METHOD OF PRODUCING 6-METHYLENO-16α,17α-CYCLOHEXANOPREGN-4-ENE-3,20-DIONE | 2014 |
|
RU2566366C1 |
17α-ACETOXY-3β-HEXANOYLOXY-6-METHYLPREGNA-4,6-DIEN-20-ON WITH GESTAGENIC, CONTRACEPTIVE AND ANTITUMOR ACTIVITY, AND THE METHOD OF ITS OBTAINING | 2018 |
|
RU2683953C1 |
METHOD OF OBTAINING 11BETA, 17 ALPHA, 21-TRIHYDROXY-16ALPHA-METHYL-9ALPHA-FLUOROPREGNA-1,4-DIENE-3,20-DIONE (DEXAMETHAZONE) FROM PHYTOSTEROL | 2013 |
|
RU2532902C1 |
0 |
|
SU412761A1 |
Authors
Dates
2013-01-20—Published
2011-12-15—Filed