Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1500946Generated: November 2, 2026

4-Chloro-1-fluoro-2-nitrobenzene → HCID 22405277, compound

https://huagongshe.com/reaction/1500946

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chloro-1-fluoro-2-nitrobenzeneHCID 67660—
ReactantDiisopropylethylamineHCID 81531—
Reactantbeta-Alanine, ethyl ester, hydrochlorideHCID 458475—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22405277HCID 2240527764.5%

Reaction Steps

A mixture of 4-chloro-1-fluoro-2-nitrobenzene (10.0 g, 57.0 mmol), ethyl 3-aminopropanoate hydrochloride (8.75 g, 57.0 mmol) and N-ethyl-N-isopropylpropan-2-amine (36.0 g, 0.285 mol) in tetrahydrofuran (150 mL) was stirred at room temperature for 16 hours. The reaction mixture was then diluted with water and then extracted with EtOAc (200 mL×3). The combined organic layers were washed with water (200 mL×3), and then dried over Na2SO4, then filtered and concentrated in vacuo. The residue was purified by flash chromatography (EtOAc:PE=1:2) to afford ethyl 3-[(4-chloro-2-nitrophenyl)amino]propanoate (10.0 g, yield: 64.5%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09206191B2
Source datasetuspto-grants-2015_12
ORD IDord-f4b86992d32a4bddba0dd086a13ffa95
Source noteuspto-grants-2015_12