HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2203124Generated: October 30, 2026
L-Valine → (2S)-2-((methoxycarbonyl)amino)-3-methylbutanoic acid
https://huagongshe.com/reaction/2203124
Participants
| Role | Name | HCID | Charge |
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| Reactant | L-Valine | HCID 6287 | — |
| Reactant | Methyl chloroformate | HCID 6586 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Solvent | Water | HCID 962 | — |
| Product | (2S)-2-((methoxycarbonyl)amino)-3-methylbutanoic acid | HCID 10942966 | 93% |
Reaction Steps
Methylchloroformate (14.5 mL, 0.188 mol) was added over 15 min to a cooled (0-6° C.) mixture of (S)-2-amino-3-methyl-butyric acid (20.0 g, 0.171 mol), NaOH (6.80 g, 0.171 mol) and sodium carbonate (18.1 g, 0.171 mol) in water (200 mL). The cooling bath was removed and the mixture was stirred at ambient temperature overnight. Conc. aqueous HCl (30 mL) was added to the reaction mixture to adjust pH to ˜1. A solid formed and the mixture was stirred for 90 min. The mixture was filtered and the solid was dried overnight under reduced pressure at 40° C. t to provide the title intermediate (27.8 g, 93% yield). 1H NMR (CD3OD, 400 MHz) δ (ppm) 4.87 (br. s, 2H), 4.05 (d, J=5.49, 1H), 3.65 (s, 3H), 2.25-2.05 (m, 1H), 0.98 (d, J=6.87, 3H), 0.94 (d, J=6.87, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09365549B2 |
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| Source dataset | uspto-grants-2016_06 |
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| ORD ID | ord-7875122d5ee847e5a8dbd36dd276a304 |
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| Source note | uspto-grants-2016_06 |
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