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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 69111Generated: October 25, 2026

Hydrochloric Acid → Tert-butyl 2-(4-bromo-2-nitrobenzoyl)-3-oxobutanoate

https://huagongshe.com/reaction/69111

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTert-butyl acetoacetateHCID 15538—
ReactantMagnesium ChlorideHCID 5360315—
Reactant4-Bromo-2-nitrobenzoyl chlorideHCID 18919880—
SolventWaterHCID 962—
SolventPyridineHCID 1049—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductTert-butyl 2-(4-bromo-2-nitrobenzoyl)-3-oxobutanoateHCID 8669431564%

Reaction Conditions

Temperature-8 °C

Reaction Steps

Under a nitrogen atmosphere, to a suspension of 2.28 g of magnesium chloride in 50 mL of tetrahydrofuran was added 3.80 g of tert-butyl 3-oxobutanoate at room temperature. The mixture was cooled to −8° C., and 3.9 mL of pyridine was added thereto, followed by stirring at the same temperature for 30 minutes, warming to room temperature, and further stirring for 30 minutes. The mixture was cooled to −8° C., and a solution of 5.3 g of 4-bromo-2-nitrobenzoyl chloride in 20 mL of tetrahydrofuran was added thereto, followed by stirring at the same temperature for 1 hour, warming to room temperature, and further stirring for 1.5 hours. The mixture was poured into a mixture of water and ethyl acetate, and adjusted to pH 3 with concentrated hydrochloric acid. The aqueous layer was separated, and then the organic layer was washed with a saturated aqueous sodium hydrogen carbonate solution and saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure to obtain 4.95 g of tert-butyl 2-(4-bromo-2-nitrobenzoyl)-3 -oxobutanoate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08822448B2
Source datasetuspto-grants-2014_09
ORD IDord-2785f0f145504683ba851c929693a5f8
Source noteuspto-grants-2014_09