HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trimethyl orthoformate → 3-Ethylenedioxy-11beta-fluoro-7alpha-methylestr-5(10)-en-17beta-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trimethyl orthoformate | HCID 9005 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Reactant | 11beta-Fluoro-17beta-hydroxy-7alpha-methylestr-4-en-3-one | HCID 9904638 | — |
| Solvent | Ethylene Glycol | HCID 174 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 3-Ethylenedioxy-11beta-fluoro-7alpha-methylestr-5(10)-en-17beta-ol | HCID 86597450 | — |
Reaction Steps
3.63 ml of ethylene glycol and 1.82 ml of trimethyl orthoformate and 23.6 ml of para-toluenesulfonic acid hydrate were added to a solution of 500 mg of 11β-fluoro-17β-hydroxy-7α-methyl-estr-4-en-3-one (I) in 6.35 ml of dichloromethane. The reaction mixture was stirred for 20 hours at room temperature. Then, it was mixed with sodium carbonate solution, diluted with ethyl acetate, washed neutral, dried on sodium sulfate, concentrated by evaporation in a vacuum and chromatographed on silica gel with hexane/ethyl acetate. 170 mg of 3-ethylenedioxy-11β-fluoro-7α-methylestr-5(10)-en-17β-ol (C), which contained portions of double-bond-isomeric 3-ethylenedioxy-11β-fluoro-7α-methylestr-5-en-17β-ol (C), was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07361645B2 |
| Source dataset | uspto-grants-2008_04 |
| ORD ID | ord-855d177f12974593abd7ebbbd9a30865 |
| Source note | uspto-grants-2008_04 |