HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sulfuric Acid → 4,17beta-Dihydroxy-14alpha,15alpha-methylene-androst-4-ene-3-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 17beta-Hydroxy-4,5-epoxy-14alpha,15alpha-methylene-androstan-3-one | HCID 87828496 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 4,17beta-Dihydroxy-14alpha,15alpha-methylene-androst-4-ene-3-one | HCID 15513338 | — |
Reaction Steps
An epoxide mixture (3.5 g), 17β-hydroxy-4,5-epoxy-14α,15α-methylene-androstan-3-one, (step 1) is dissolved in 50 mL of acetic acid, which contains 2% by volume of concentrated sulfuric acid. The solution is allowed to stand for 3 days at 10° C. After that, it is treated with 200 mL ethyl acetate and neutralized with sodium carbonate solution. The organic phase is dried and concentrated. The residue is dissolved in 100 mL of methanol, treated with 4 g of potassium hydroxide, refluxed for 1 hour and then cooled. After neutralization with 50% acetic acid, it is poured into 1 L of water and the crystals are filtered off with suction, 4,17β-Dihydroxy-14α,15α-methylene-androst-4-ene-3-one being obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06710039B1 |
| Source dataset | uspto-grants-2004_03 |
| ORD ID | ord-c8a352c0a05e41e0b43ed42a8dd9ad40 |
| Source note | uspto-grants-2004_03 |