HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 72046Generated: October 28, 2026
Water → 2-(((Tert-butoxy)carbonyl)amino)-3-methoxy-3-methylbutanoic acid
https://huagongshe.com/reaction/72046
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | N-Boc-(+-)-2-amino-3-hydroxy-3-methylbutanoic acid | HCID 13756005 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-(((Tert-butoxy)carbonyl)amino)-3-methoxy-3-methylbutanoic acid | HCID 23138410 | 94% |
Reaction Steps
2-tert-Butoxycarbonylamino-3-hydroxy-3-methyl-butyric acid (1.0 g, 4.29 mmol) was dissolved in THF (14 mL) and cooled to 0° C. in an external ice/brine bath. MeI (2.13 mL, 34.3 mmol) was added at 0° C. Solid NaH (60% dispersion in mineral oil, 0.514 g, 12.87 mmol) was added slowly 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 diluted in ethyl acetate and water was added slowly with stirring. The quenched mixture was concentrated in vacuo and partitioned between diethyl ether and water. The ether layer was extracted with sodium bicarbonate twice. The combined bicarbonate layers were acidified with aqueous citric acid to pH 3 and extracted three times with ethyl acetate. The combined ethyl acetate layers were washed with water, sodium thiosulfate, water, dried with sodium sulfate and concentrated to yield 2-tert-Butoxycarbonylamino-3-methoxy-3-methyl-butyric acid (0.99 g, 94%) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08822430B2 |
|---|
| Source dataset | uspto-grants-2014_09 |
|---|
| ORD ID | ord-db5f696c6e33465cbe4cbb21a7ef267b |
|---|
| Source note | uspto-grants-2014_09 |
|---|