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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2272618Generated: October 27, 2026

4-Amino-2-chlorobenzonitrile → 5-((3-Chloro-4-cyanophenyl)amino)-2-methyl-5-oxopentanoic acid

https://huagongshe.com/reaction/2272618

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Amino-2-chlorobenzonitrileHCID 88728—
Reactantdihydro-3-methyl-2H-pyran-2,6(3H)-dioneHCID 3015571—
Reactant5-((3-Chloro-4-cyanophenyl)amino)-4-methyl-5-oxopentanoic acidHCID 86729776—
SolventTolueneHCID 1140—
SolventSodium chloride; waterHCID 57417360—
Product5-((3-Chloro-4-cyanophenyl)amino)-2-methyl-5-oxopentanoic acidHCID 8672977539.1%

Reaction Steps

A solution of 3-methyldihydro-2H-pyran-2,6(3H)-dione (876 mg, 6.84 mmol), 4-amino-2-chlorobenzonitrile (1044 mg, 6.84 mmol) and TEA (0.953 mL, 6.84 mmol) in toluene (10 mL) was stirred at 70° C. for 3 hr. To the reaction mixture was added brine at room temperature, and the mixture was extracted with ethyl acetate. The organic layer was washed with water and saturated brine, and dried, and the solvent was evaporated under reduced pressure. The obtained residue was purified by COOH-silica gel column chromatography (solvent gradient; 10 to 100% ethyl acetate/hexane) to give a mixture (750 mg, 2.67 mmol, 39.1%) of 5-((3-chloro-4-cyanophenyl)amino)-2-methyl-5-oxopentanoic acid and 5-((3-chloro-4-cyanophenyl)amino)-4-methyl-5-oxopentanoic acid, as a colorless powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09120776B2
Source datasetuspto-grants-2015_09
ORD IDord-58618add03cf49a49c447cb3508cdb67
Source noteuspto-grants-2015_09