Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Bromic acid | HCID 24445 | — |
| Reactant | HCID 86623004 | HCID 86623004 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 87489997 | HCID 87489997 | — |
Reaction Steps
4-Amino-(S)-1,2-butandiol bromate 6 (0.537 mol, 100 g) and an acetic acid solution (185 g) with 33% bromic acid dissolved therein were added to a 500□ round-bottom flask and the mixture was agitated at 40° C. for 2 hours. After the preparation of an intermediate was confirmed by Thin Layer Chromatography (TLC), anhydrous ethanol (285 g) was added thereto. The reaction mixture was agitated under reflux for 3 hours to complete the reaction and then concentrated under reduced pressure to completely remove the solvent, thereby obtaining 115 g of crude 4-amino-1-bromo-(S)-2-butanol bromate 7.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07652152B2 |
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| Source dataset | uspto-grants-2010_01 |
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| ORD ID | ord-c7bf409fb99342e3837e8eff8154feda |
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| Source note | uspto-grants-2010_01 |
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