Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Potassium Chloride | HCID 4873 | — |
| Reactant | Fuming sulfuric acid | HCID 24681 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 21253725 | HCID 21253725 | — |
| Product | HCID 21253733 | HCID 21253733 | — |
Reaction Steps
59.4 g (0.2 mol) of 5-(2′-aminophenyl)-3-[2-(2-hydroxyethylsulfonyl)ethyl]-1,2,4-oxadiazole were added at 10-15° C. to 100% strength sulfuric acid and stirred in at 40° C. for 1 h. 240 ml of 24% strength by weight oleum were then added at 40° C. a little at a time over 20 h. After heating at 60° C. for 8 h, the reaction solution was poured onto ice, the pH was adjusted to pH 4-5 with sodium bicarbonate, and the product was salted out with 500 g of potassium chloride to afford 95.3 g of 5-(2′-amino-5′-sulfophenyl)-3-[2-(2-hydroxyethylsulfonyl)ethyl]-1,2,4-oxadiazole.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06197941B1 |
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| Source dataset | uspto-grants-2001_03 |
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| ORD ID | ord-686a0cb940eb4bb2950eae328126ab22 |
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| Source note | uspto-grants-2001_03 |
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