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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 57408Generated: October 27, 2026

Potassium Carbonate → tert-Butyl (2S)-but-3-yn-2-ylcarbamate

https://huagongshe.com/reaction/57408

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactanttert-butyl N-((2S)-1-oxopropan-2-yl)carbamateHCID 7015728—
Reactant(1E)-1-diazo-1-dimethoxyphosphorylpropan-2-oneHCID 136023029—
SolventMethanolHCID 887—
SolventSodium ChlorideHCID 5234—
SolventEthyl AcetateHCID 8857—
Producttert-Butyl (2S)-but-3-yn-2-ylcarbamateHCID 1098667753%

Reaction Steps

A solution of (S)-tert-butyl(1-oxopropan-2-yl)carbamate (500 mg, 2.89 mmol), dimethyl(1-diazo-2-oxopropyl)phosphonate (610 mg, 3.18 mmol, 1.1 equiv), and potassium carbonate (638 mg, 4.62 mmol, 1.6 equiv) in methanol (14.4 mL) was stirred at room temperature for 18 hours. The reaction was then diluted with ethyl acetate (30 mL) and saturated aqueous sodium chloride (40 mL). The layers were separated and the aqueous layer was extracted with ethyl acetate (30 mL) and the combined organic extracts were dried over Na2SO4, filtered and concentrated. Silica gel column chromatography (20% EtOAc in Heptane) provided (S)-tert-butyl but-3-yn-2-ylcarbamate (0.258 g, white solid) in 53% yield. 1H NMR (400 MHz, CDCl3) δ 4.49 (m, 1H), 2.26 (d, J=2.2 Hz, 1H), 1.46 (s, 9H), 1.41 (d, J=6.8 Hz, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09434719B2
Source datasetuspto-grants-2016_09
ORD IDord-3b3c45eaca954158b78654fa10bad086
Source noteuspto-grants-2016_09