HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1471002Generated: October 29, 2026
Hydrochloric Acid → (2S)-2-((methoxycarbonyl)amino)-3-methylbutanoic acid
https://huagongshe.com/reaction/1471002
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | L-Valine | HCID 6287 | — |
| Reactant | Methyl chloroformate | HCID 6586 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | (2S)-2-((methoxycarbonyl)amino)-3-methylbutanoic acid | HCID 10942966 | 50.4% |
Reaction Steps
A mixture of (S)-2-amino-3-methylbutanoic acid (10.0 g, 85.0 mmol), NaOH (3.41 g, 85.0 mmol) and NaHCO3 (4.7 g, 44.4 mmol) in H2O (85 mL) was cooled to 0° C. A mixture of methyl chloroformate (7.3 mL, 94.0 mmol) dissolved in Et2O (40 mL) was slowly added to the aqueous S mixture and stirred for 20 hours coming to ambient temperature. Mixture was adjusted to pH 2.0 with HCl (conc). The mixture was extracted with CH2Cl2 (3×100 mL) and then dried (MgSO4), filtered and concentrated to afford 7.5 g (50%) of the title compound. MS (ESI) m/z 176 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09006387B2 |
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| Source dataset | uspto-grants-2015_04 |
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| ORD ID | ord-8f062eac550c4d5c9cafda1bc110c953 |
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| Source note | uspto-grants-2015_04 |
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