HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 55757Generated: October 27, 2026
L-Valine → (2S)-2-((methoxycarbonyl)amino)-3-methylbutanoic acid
https://huagongshe.com/reaction/55757
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | L-Valine | HCID 6287 | — |
| Reactant | Methyl chloroformate | HCID 6586 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Product | (2S)-2-((methoxycarbonyl)amino)-3-methylbutanoic acid | HCID 10942966 | — |
Reaction Steps
To L-Valine (20 g, 167.3 mmol) in a stirred aqueous NaOH (1M, 167 mL) solution in a round bottom flask (1 L), sodium carbonate (8.866 g, 83.6 mmol) was added. The flask was cooled to 0° C. in an ice-water bath. Methyl chloroformate (17.4 g, 184 mmol) was added drop wise and the reaction mixture was allowed to stir for 15 hours and reach room temperature. The reaction mixture was separated with ether (3×200 mL), and the aqueous layer was contained in a round bottom flask and cooled in a ice-water bath. Concentrated HCl (aq) was added drop wise until pH 2. The mixture was brought to room temperature and extracted with dichloromethane (3×200 mL). The organic layers were pooled, dried (sodium sulfate), and the solids were removed by filtration. The solvents of the filtrate were removed under reduced pressure to afford a white solid. The white solid was further dried in vacuum (25.3 g, 86%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09433609B2 |
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| Source dataset | uspto-grants-2016_09 |
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| ORD ID | ord-1f007307ec0949e3a7a1cc5f7472b763 |
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| Source note | uspto-grants-2016_09 |
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