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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 588784Generated: October 28, 2026

Ethyl bromoacetate → Ethyl 2-(4,5-dichloro-2-ethylphenylamino)acetate

https://huagongshe.com/reaction/588784

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantSodium hydrideHCID 24758—
Reactant4,5-Dichloro-2-ethylbenzenamineHCID 21336848—
SolventDimethylformamideHCID 6228—
ProductEthyl 2-(4,5-dichloro-2-ethylphenylamino)acetateHCID 11761067444.7%

Reaction Steps

To a stirring solution of 4,5-dichloro-2-ethylbenzenamine (600 mg, 3.15 mmol) in DMF at 0° C., NaH (150 mg, 3.78 mmol) was added in portions. After stirring for 30 min, ethyl 2-bromoacetate (789 mg, 4.74 mmol) was added to the mixture. The resulting mixture was stirred at 120° C. for 16 h. The mixture was allowed to cool to room temperature, poured into ice-water and extracted with ethyl acetate. The organic layer was washed with brine, dried over Na2SO4 and concentrated. The residue was purified by flash column chromatography on silica gel (petroleum ether/ethyl acetate=5:1) to afford the desired product (380 mg, 44.7% yield) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09227978B2
Source datasetuspto-grants-2016_01
ORD IDord-0fed17fce140469bbc32c701a81c0810
Source noteuspto-grants-2016_01