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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriacetoxyperiodinaneHCID 159087—
Reactanttert-butyl N-((2R)-1-hydroxypropan-2-yl)carbamateHCID 13200309—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
Producttert-butyl N-((2R)-1-oxopropan-2-yl)carbamateHCID 1091004985.3%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09221826B2
Source datasetuspto-grants-2015_12
ORD IDord-cc5a49085c76434e94cf9989d597aa21
Source noteuspto-grants-2015_12