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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 659135Generated: October 31, 2026

Triethylamine → Tert-butyl 3-methyl-1-oxobutan-2-ylcarbamate

https://huagongshe.com/reaction/659135

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantN-Boc-DL-valinolHCID 545981—
SolventDimethyl SulfoxideHCID 679—
ProductTert-butyl 3-methyl-1-oxobutan-2-ylcarbamateHCID 54598572.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 1.75 g of tert-butyl 1-hydroxy-3-methylbutan-2-ylcarbamate (Formula 20) in 25 mL of DMSO was added 3.6 mL of triethylamine. The solution was cooled to 0° C. and 4.1 grams of sulfur trioxide pyridine complex in 25 mL of DMSO was added. The reaction mixture was stirred at room temperature for 1 hour. Then, the mixture was poured onto ice-water and extracted with ethyl acetate. The organic layers were washed with 10% acetic acid, water, 5% sodium bicarbonate, and brine, dried over sodium sulfate and concentrated. Column chromatography (30% ethyl acetate/hexane) gave 1.25 g of tert-butyl 3-methyl-1-oxobutan-2-ylcarbamate (Formula 21) as a clear oil. 1H NMR (300 MHz, CDCl3) δ 0.95 (d, J=7.32 Hz, 3H), 1.03 (d, J=6.83 Hz, 3H), 1.45 (s, 9H), 2.27-2.29 (m, 1H), 4.24-4.26 (m, 1H), 9.65 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08080570B2
Source datasetuspto-grants-2011_12
ORD IDord-58746b33dbe24035af15d1c504d049a3
Source noteuspto-grants-2011_12