HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoic anhydride → methyl(11R,12S,13E,15S)-9-benzoyloxy-11,15-bis(tert-butyldimethylsiloxy)-7-thiaprosta-8,13-dienoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoic anhydride | HCID 7167 | — |
| Reactant | (3S)-1-Iodo-3-(tert-butyldimethylsilyloxy)-1-octene | HCID 11111369 | — |
| Reactant | (4R)-tert-butyldimethylsiloxy-2-(5-methoxycarbonylpentylthio)-2-cyclopenten-1-one | HCID 131720587 | — |
| Reactant | HCID 178418306 | HCID 178418306 | — |
| Reactant | C6H9Cu | HCID 178418419 | — |
| Solvent | Hexamethylphosphorous triamide | HCID 15355 | — |
| Product | methyl(11R,12S,13E,15S)-9-benzoyloxy-11,15-bis(tert-butyldimethylsiloxy)-7-thiaprosta-8,13-dienoate | HCID 22883804 | 55.4% |
Reaction Steps
Using as the materials and reagents (1E,3S)-1-iodo-3-(tert-butyldimethylsiloxy)-1-octene (442 mg, 1.2 mmol), tert-butyllithium (1.54 mol/l, 1.56 ml, 2.4 mmol), 1-hexynylcopper (174 mg), hexamethylphosphorous triamide (436 μl), (4R)-tert-butyldimethylsiloxy-2-(5-methoxycarbonyl-pentylthio)-2-cyclopenten-1-one (373 mg, 1.0 mmol), and benzoic anhydride (661 mg), the same procedure was performed as in Example 1 to obtain methyl(11R,12S,13E,15S)-9-benzoyloxy-11,15-bis(tert-butyldimethylsiloxy)-7-thiaprosta-8,13-dienoate (239 mg, 33%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05731452 |
| Source dataset | uspto-grants-1998_03 |
| ORD ID | ord-76d32aafd0e142d0832c397f95f52a05 |
| Source note | uspto-grants-1998_03 |