Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Pentene | HCID 8004 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | MAGNESIUM SILICATE (synthetic) | HCID 61680 | — |
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | 9-Borabicyclo(3.3.1)nonane | HCID 78966 | — |
| Reactant | HCID 86754854 | HCID 86754854 | — |
| Product | HCID 15867799 | HCID 15867799 | 38% |
Reaction Steps
1-pentene (110 μl, 1.0 mmol) in tetrahydrofuran (3 mL) was ice-cooled, then 9-borabicyclo[3,3,1]nonane (9-BBN, 0.5M THF solution, 2.0 mL, 1.05 mmoL) was added. This was agitated for 6 hours while gradually raising the reaction temperature to room temperature. Further, to this were added methyl (11R,12S,13E,15S,17R)-9-trifluoromethanesulfonyloxy-11,15-bis(tert-butyldimethylsiloxy)-17,20-dimethyl-7-thiaprosta-8,13-dienoic acid (205 mg, 0.264 mmol), bistriphenylphosphinepalladiumchloride (140 mg, 0.2 mmol), and tripotassium phosphate (255 mg, 1.2 mmol) in tetrahydrofuran (5 mL) suspension. The reaction mixture was agitated at 60° C. for 15 hours. The reaction solution was cooled, then subjected to Florisil column chromotography to remove the metal complexes. The resultant solution was concentrated under reduced pressure, then was purified by silica gel column chromotography (2 to 4% ethyl acetate/hexane) to obtain methyl (11R,12S,13E,15S,17R)-9-pentyl-11,15-bis(tert-butyldimethylsiloxy)-17,20-dimethyl-7-thiaprosta-8,13-dienoate (71 mg, 38%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05990346 |
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| Source dataset | uspto-grants-1999_11 |
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| ORD ID | ord-24f587d066a6426aae77f8aa305c5b36 |
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| Source note | uspto-grants-1999_11 |
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