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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 588506Generated: October 25, 2026

Pyridine → (R)-tert-butyl 1-(hydroxyimino)propan-2-ylcarbamate

https://huagongshe.com/reaction/588506

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantHydroxyamine hydrochlorideHCID 443297—
Reactanttert-butyl N-((2R)-1-oxopropan-2-yl)carbamateHCID 10910049—
SolventMethanolHCID 887—
Product(R)-tert-butyl 1-(hydroxyimino)propan-2-ylcarbamateHCID 86657336157.4%

Reaction Steps

A mixture of (R)-tert-butyl 1-oxopropan-2-ylcarbamate (28.0 g, 81.0 mmol), hydroxylamine hydrochloride (11.2 g, 81.0 mmol), pyridine (60 mL), MeOH (100 mL) was stirred at rt overnight. The solvent was then evaporated. To the residue was added water (100 mL) and the mixture was extracted with DCM (3×200 mL). The combined organic phases were dried (Na2SO4) and concentrated. The crude residue was purified by flash column chromatography (petroleum ether: EtOAc, 4:1) to give (R)-tert-butyl 1-(hydroxyimino)propan-2-ylcarbamate (24.0 g, 79%). 1H NMR (DMSO-d6, 400 MHz) δ 10.63 (s, 1H), 7.20 (d, J=5.2 Hz, 1H), 4.12 (m, 1H), 1.38 (s, 9H), 1.15 (d, J=6.8 Hz, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09227951B2
Source datasetuspto-grants-2016_01
ORD IDord-d880de63941f4bdaa69283c12c2a1f37
Source noteuspto-grants-2016_01