HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2071345Generated: October 31, 2026
Hydrochloric Acid → 9alpha,15-Dihydroxyprostanoic acid
https://huagongshe.com/reaction/2071345
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | AY 22093 | HCID 193037 | — |
| Reactant | Lithium perhydro-9b-boraphenalylhydride | HCID 70418318 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 9alpha,15-Dihydroxyprostanoic acid | HCID 18594815 | — |
Reaction Steps
To a solution of 433 mg. of 15-hydroxy-9-oxoprostanoic acid (Example 186) in 4.5 ml. of tetrahydrofuran, stirred in an ice-bath under nitrogen atmosphere, is added dropwise 3.7 ml. of 0.76 M lithium perhydro-9b-boraphenalylhydride. After 40 minutes at 0° C. there is added 1.62 ml. of 3N sodium hydroxide followed by 1.62 ml. of 30% hydrogen peroxide. Ether is added and the resulting solution is acidified with 2N hydrochloric acid. The ether layer is washed several times with saturated sodium chloride solution, dried with anhydrous magnesium sulfate and taken to dryness to give 300 mg. (70%) of waxy solid; nmr 3H singlet δ 4.64 (hydroxyl and carboxyl protons), 1 H singlet 4.22 (9β-carbinolic proton, 80%), 1 H singlet 3.88 (9α-carbinolic protons, 20%), 1 H singlet 3.61 (15-carbinolic proton), and 3 H distorted triplet 0.90 (terminal methyl).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04046787 |
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| Source dataset | uspto-grants-1977_09 |
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| ORD ID | ord-c244fad941a14f3eba4384d41101d695 |
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| Source note | uspto-grants-1977_09 |
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