HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 239737Generated: October 30, 2026
Aminoisobutyric acid → Alanine, 2-methyl-N-(3-sulfopropyl)-
https://huagongshe.com/reaction/239737
Participants
| Role | Name | HCID | Charge |
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| Reactant | Aminoisobutyric acid | HCID 6119 | — |
| Reactant | Propane sultone | HCID 14264 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | Alanine, 2-methyl-N-(3-sulfopropyl)- | HCID 11160456 | — |
Reaction Steps
To a cold (5° C.) mixture of 2-aminoisobutyric acid (2.0 g, 19.4 mmol), NaOH (776 mg, 19.4 mmol) in 1,4-dioxane (10 mL) and water (4 mL) was added via syringe pump (over a 4-hour period), a solution 1,3-propane sultone (2.02 g, 16.2 mmol) in 1,4-dioxane (total: 4 mL). The solution was stirred at room temperature for 2 hours before it was allowed to warm up to room temperature. The reaction mixture was stirred under these conditions overnight. The solvent was evaporated under reduced pressure. The resultant solid material was recrystallized from 5% water/EtOH. The resulting solid was dissolved in water; and the aqueous solution was passed through an ion exchange column (Dowex 50WX 8, 100 g, solvent: water). The solvent was evaporated under reduced pressure. The product was lyophilized to afford Compound DI (880 mg, 28%). 1H NMR (D2O, 500 MHz) 8 ppm 3.00 (t, 2H, J=7.6 Hz), 2.91 (t, 2H, J=7.3 Hz), 2.01 (m, 2H), 1.34 (s, 6H). 13C NMR (D2O, 125 MHz) 8 ppm 176.93, 63.89, 48.13, 42.04, 22.15, 21.86. ES-MS 224 (M−1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08642801B2 |
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| Source dataset | uspto-grants-2014_02 |
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| ORD ID | ord-6169b3c80b8e429c9c8a888cf7005a0b |
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| Source note | uspto-grants-2014_02 |
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