Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Potassium Chloride | HCID 4873 | — |
| Reactant | 4-(Dimethylamino)Benzaldehyde | HCID 7479 | — |
| Reactant | Boric Acid | HCID 7628 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Tosylchloramide | HCID 31388 | — |
| Reactant | L-Proline, 1-hydroxy | HCID 22795248 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 2-Methoxyethanol | HCID 8019 | — |
| Product | L-Hydroxyproline | HCID 5810 | — |
| Product | 4-(Dimethylamino)Benzaldehyde | HCID 7479 | — |
| Product | Boric Acid | HCID 7628 | — |
| Product | Tosylchloramide | HCID 31388 | — |
Reaction Steps
A boric acid buffer was prepared by dissolving 6.18 g of boric acid and 22.5 g of KCl in distilled water, adjusting at pH 8.7 with potassium hydroxide and making the total volume 100 ml. A chloramine T solution was prepared by dissolving 1.41 g of chloramine T (NACALAITESQUE, Catalog No.080-05) in 25 ml of 2-methoxyethanol (NACALAITESQUE, Catalog No.153-10). A p-dimethylaminobenzaldehyde solution was prepared by dissolving 12 g of p-dimethylaminobenzaldehyde (NACALAITESQUE, Catalog No.128-16) in 20 ml of ethanol followed by adding a mixture of 2.74 ml of concentrated sulfuric acid and 20 ml of ethanol slowly to the solution with cooling on ice. A hydroxyproline conventional solution was prepared by dissolving 3 mg of hydroxy-L-proline (NACALAITESQUE, Catalog No.188-17) in 1 ml of distilled water (3 mg/ml).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08404652B2 |
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| Source dataset | uspto-grants-2013_03 |
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| ORD ID | ord-71abd08380f64e7f8f88462895fd8297 |
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| Source note | uspto-grants-2013_03 |
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