Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Phosphate | HCID 1061 | — |
| Reactant | Ammonium Sulfate | HCID 6097028 | — |
| Reactant | HCID 15867800 | HCID 15867800 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 15867801 | HCID 15867801 | 28.3% |
Reaction Steps
To methyl (11R,12S,13E,15S,17R)-9-pentyl-11,15-dihydroxy-17,20-dimethyl-7-thiaprosta-8,13-dienoate (20 mg, 0.042 mmol) in acetone (1 mL) was added pH 8 phosphate buffer (5 mL). To this was further added esterase containing solution (derived from pig's liver, made by Sigma Co., 50 μl). The solution was agitated at room temperature for 24 hours. Dilute hydrochloric acid was added to the reaction solution to make the solution pH 4. Further, the solution was made saturated by ammonium sulfate, then the desired product was extracted with ethyl acetate. The extract was washed with brine, then was dried over anhydrous sodium sulfate. The solution was concentrated under reduced pressure, then subjected to thin layer chromotography for separation (development solution: ethyl acetate) to obtain (11R,12S,13E,15S,17R)-9-pentyl-11,15-dihydroxy-17,20-dimethyl-7-thiaprosta-8,13-dienoic acid (5.4 mg, 14%).
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-ca534c053a38497cb302dc00cc9017fe |
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| Source note | uspto-grants-1999_11 |
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