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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 522368Generated: October 29, 2026

Ethyl Acetate → 3-(4-Bromoanilino)-3-oxopropanoic acid

https://huagongshe.com/reaction/522368

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantSodium HydroxideHCID 14798—
Reactant3-(4-Bromoanilino)-3-oxopropanoic acid ethyl esterHCID 12324957—
SolventTetrahydrofuranHCID 8028—
Product3-(4-Bromoanilino)-3-oxopropanoic acidHCID 3796450—

Reaction Steps

The product of Step 1 (16.63 g) was dissolved in THF (150 mL) and 2N NaOH (145 mL) was added over 15 minutes. The reaction was stirred for 24 hours. The reaction mixture was concentrated to remove the THF. Diethyl ether (20 mL) was added and the layers were separated. The aqueous layer was acidified to pH=2.2 with 1N HCl which resulted in the precipitation of solids. Ethyl acetate was added until the solids were dissolved and the layers were separated. The organic extract was dried with sodium sulfate, filtered and concentrated to give 14.7 g of a cake.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09328138B2
Source datasetuspto-grants-2016_05
ORD IDord-df6b92635cf1422db4d2ce2c10a12b86
Source noteuspto-grants-2016_05