HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 72047Generated: October 28, 2026
Hydrochloric Acid → 3-Methoxy-2-methoxycarbonylamino-3-methyl-butyric acid
https://huagongshe.com/reaction/72047
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methyl chloroformate | HCID 6586 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-(((Tert-butoxy)carbonyl)amino)-3-methoxy-3-methylbutanoic acid | HCID 23138410 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 3-Methoxy-2-methoxycarbonylamino-3-methyl-butyric acid | HCID 20131893 | 65% |
Reaction Steps
2-tert-Butoxycarbonylamino-3-methoxy-3-methyl-butyric acid was dissolved in dioxane (40 mL) and HCl (4N in dioxane, 5.4 mL, 21.6 mmol) was added at room temperature. The resulting solution was stirred at room temperature for 18 hours and the concentrated to dryness. The solid was dissolved in THF (14 mL) and cooled to 0° C. in an external ice/brine bath. Aqueous sodium hydroxide (6.25M, 1.9 mL, 11.76 mmol) and methyl chloroformate (0.5 mL, 5.88 mmol) were added at 0° C. Upon completion of the addition, the solution was removed from the ice bath and allowed to warm to room temperature, and stirred. After 18 hours, the crude reaction mixture was adjusted to pH 1 with 1N HCl and extracted twice with diethyl ether. The combined organic layers were washed with brine, dried with magnesium sulfate and concentrated to give 3-Methoxy-2-methoxycarbonylamino-3-methyl-butyric acid (0.653 g, 65%) as an off-white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08822430B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-0ef47b88587a45efa13597a698c3acd0 |
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| Source note | uspto-grants-2014_09 |
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