HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1053883Generated: November 1, 2026
L-Valine → (2S)-2-((methoxycarbonyl)amino)-3-methylbutanoic acid
https://huagongshe.com/reaction/1053883
Participants
| Role | Name | HCID | Charge |
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| Reactant | L-Valine | HCID 6287 | — |
| Reactant | Methyl chloroformate | HCID 6586 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | (2S)-2-((methoxycarbonyl)amino)-3-methylbutanoic acid | HCID 10942966 | 94% |
Reaction Steps
To (S)-2-amino-3-methylbutanoic acid (57 g, 487 mmol) dissolved in dioxane (277 mL) was added a 2 N aqueous sodium hydroxide solution (803 mL, 1606 mmol) followed by the dropwise addition of methyl chloroformate (75 mL, 973 mmol) over 1 hour which caused warming of the solution to occur. After the addition, the mixture was heated at 60° C. for 22 hours, then cooled and extracted with dichloromethane (400 mL). The resultant aqueous layer was cooled in an ice bath, and then 12 N hydrochloric acid was added dropwise until the pH was 2. The resultant mixture was stirred at 0° C. for 2 hours, and then the resultant solid was collected by vacuum filtration, and dried in a vacuum oven to provide 80 g (94%) of the title compound as a colorless solid. 1H NMR (400 MHz, DMSO-d6) δ ppm 12.50 (bs, 1H), 7.34 (d, J=8.6 Hz, 1H), 3.84 (dd, J=8.6, 6.0 Hz, 1H), 3.54 (s, 3H), 2.03 (m, 1H), 0.86 (t, J=7.0 Hz, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09394279B2 |
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| Source dataset | uspto-grants-2016_07 |
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| ORD ID | ord-fb3baea16e824b1e90d23b5b3e306591 |
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| Source note | uspto-grants-2016_07 |
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