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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2104310Generated: November 1, 2026

Dimethyl Sulfoxide → tert-butyl N-(2-methyl-4-oxobutan-2-yl)carbamate

https://huagongshe.com/reaction/2104310

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
Reactanttert-Butyl (4-hydroxy-2-methylbutan-2-yl)carbamateHCID 15473340—
SolventDichloromethaneHCID 6344—
Producttert-butyl N-(2-methyl-4-oxobutan-2-yl)carbamateHCID 1178890163.6%

Reaction Conditions

Temperature-78 °C

Reaction Steps

DMSO (1.22 mL, 17.2 mmol) was added to a solution of oxalyl chloride (1.1 mL, 12.9 mmol) at −78° C. in dichloromethane (15 mL). The mixture was stirred for 15 min at −78° C. A solution of 3-hydroxy-1,1-dimethylpropylcarbamic acid tert-butyl ester (1.75 g, 8.6 mmol) in dichloromethane (10 mL) was added dropwise over a period of 15 min. The solution was stirred at −78° C. for another 15 min. Triethylamine (6.0 mL, 43 mmol) was added. The solution was stirred at −78° C. for 5 min and then warmed to room temperature. The solution was diluted with dichloromethane (100 mL) and extracted with 1N hydrochloric acid (100 mL). The aqueous phase was extracted with dichloromethane (50 mL). The combined organic layers were washed with saturated sodium hydrogen carbonate solution (100 mL) and dried over magnesium sulfate. The solvent was removed in vacuo. The crude product was purified by column chromatography on silica (140 g) with ethyl acetate/heptane (1:3) to give 1.10 g of 3-(tert-butoxycarbonylamino)-3-methylbutanal.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07576062B2
Source datasetuspto-grants-2009_08
ORD IDord-8613939ff0024ea6a37199c98a838854
Source noteuspto-grants-2009_08