HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 78732Generated: October 26, 2026
(S)-2-(Boc-Amino)-N-methoxy-n-methylbutyramide → tert-butyl N-((2S)-1-oxobutan-2-yl)carbamate
https://huagongshe.com/reaction/78732
Participants
| Role | Name | HCID | Charge |
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| Reactant | (S)-2-(Boc-Amino)-N-methoxy-n-methylbutyramide | HCID 10422029 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | tert-butyl N-((2S)-1-oxobutan-2-yl)carbamate | HCID 10241556 | — |
Reaction Steps
To a solution of LiAlH4 (0.453 g, 11.9 mmol) in Et2O (20 mL) at 0° C. was added dropwise a solution of 1,1-dimethylethyl ((1S)-1-{[methyl(methyloxy)amino]carbonyl}-propyl)carbamate (2.67 g, 10.8 mmol) in Et2O (15 mL). The reaction mixture was stirred for 30 min at 0° C. and quenched with EtOAc (6.5 mL) followed by 5% aq. potassium bisulfate (6.5 mL). The reaction mixture was washed with 1 M aq. HCl (3×10 mL), saturated aq. NaHCO3 (3×10 mL), and brine (10 mL). The organic layer was dried over Na2SO4, filtered, and concentrated in vacuo to afford the title compound as a clear, colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08841463B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-5760667bccfa440ab1833c283b8e4596 |
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| Source note | uspto-grants-2014_09 |
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