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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 366107Generated: October 31, 2026

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

https://huagongshe.com/reaction/366107

Reaction equation

Participants

RoleNameHCIDCharge
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

Dimethylsufoxide (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 numberUS06127354
Source datasetuspto-grants-2000_10
ORD IDord-d535c47c404541c68dbd12903e94f351
Source noteuspto-grants-2000_10