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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 127889Generated: October 25, 2026

2-tert-Butyl-1,3-diisopropylisourea → tert-Butyl 3-bromo-2-oxobutanoate

https://huagongshe.com/reaction/127889

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-tert-Butyl-1,3-diisopropylisoureaHCID 11041782—
Reactant3-Bromo-2-oxobutanoic acidHCID 14471256—
SolventDichloromethaneHCID 6344—
Producttert-Butyl 3-bromo-2-oxobutanoateHCID 2347014947.7%

Reaction Steps

A solution of 1.6 g (8.85 mmol) of 3-bromo-2-ketobutyric acid and 7 g (4 equivalents) of O-t-butyl-N,N'-diisopropylpseudourea in 14 ml methylene chloride is stirred overnight at room temperature. After filtration, the solution is washed with NaHCO3 and brine, dried and evaporated to an oil which is chromatographed on silica gel with benzene as eluant to give 1 g (45%) of t-butyl 3-bromo-2-ketobutyrate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04257947
Source datasetuspto-grants-1981_03
ORD IDord-c830d3d5ac4f43b8a99b12c1711f57cb
Source noteuspto-grants-1981_03