HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1507965Generated: October 30, 2026
Water → tert-butyl N-((2R)-1-oxopropan-2-yl)carbamate
https://huagongshe.com/reaction/1507965
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triacetoxyperiodinane | HCID 159087 | — |
| Reactant | tert-butyl N-((2R)-1-hydroxypropan-2-yl)carbamate | HCID 13200309 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | tert-butyl N-((2R)-1-oxopropan-2-yl)carbamate | HCID 10910049 | 85.3% |
Reaction Steps
Water (2.57 ml, 143 mmol) was added dropwise to a mixture of (R)-tert-butyl (1-hydroxypropan-2-yl)carbamate (17.85 g, 102 mmol) and Dess-Martin Periodinane (60.5 g, 143 mmol) in anhydrous DCM (500 ml) at rt under a nitrogen atmosphere. The reaction was allowed to stir at rt overnight before diluting with diethyl ether and filtering. The filtrate was evaporated in vacuo and the residue diluted with diethyl ether. The organic was then washed with a 1:1 mixture of 10% aq sodium thiosulfate solution: sat. sodium bicarbonate solution, followed by brine and water. The aqueous phase was then back extracted with one portion of diethyl ether, the combined organics were then dried (MgSO4) and evaporated in vacuo to give (R)-tert-butyl (1-oxopropan-2-yl)carbamate (15 g, 87 mmol, 85% yield) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09221826B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-cc5a49085c76434e94cf9989d597aa21 |
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| Source note | uspto-grants-2015_12 |
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