Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | HCID 178488125 | HCID 178488125 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Hydrogen Peroxide | HCID 784 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178488147 | HCID 178488147 | 69% |
Reaction Steps
0.35 g of 2-[[(3,5-dimethyl-4-methoxy-2-pyridinyl)methyl]thio]-5-methoxy-1H-benzimidazole was suspended in 5 ml of ethanol at room temperature. 0.035 g of Na2WO4·2H2O oxidation catalyst was dissolved in 0.099 g H2O2 (35% aqueous solution), and further diluted with 2 ml of water. The oxidant/catalyst solution was added to the reactant suspension dropwise so that the addition was completed in about 30 minutes while stirring at room temperature. The reaction was continued for additional 6 hours while stirring. 2 ml of 10% Na2S2O3 aqueous solution was then, added, and the resulting mixture was subjected to a reduced pressure to remove ethanol therefrom. Finally, a precipitate was formed after adding a diluted acetic acid aqueous solution to a pH value of about 8, which was filtered, water washed, and dried in vacuo to obtain Omeprazole with a yield of about 69% (LC purity>80%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07531666B2 |
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| Source dataset | uspto-grants-2009_05 |
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| ORD ID | ord-a2a48aa73f364823850070f51b06b7b0 |
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| Source note | uspto-grants-2009_05 |
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