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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 24729Generated: October 26, 2026

P-Anisidine → HCID 178492232, compound

https://huagongshe.com/reaction/24729

Reaction equation

Participants

RoleNameHCIDCharge
ReactantP-AnisidineHCID 7732—
ReactantTriethylamineHCID 8471—
Reactant1-Acetyl-3-(1-chloro-1-phenyl-methylidene)-2-indolinoneHCID 69743657—
SolventDichloromethaneHCID 6344—
ProductHCID 178492232HCID 178492232—

Reaction Steps

0.18 g (1.5 mmol) of 4-methoxyaniline and 0.2 g (0.28 mmol) of triethylamine are dissolved in 5 ml of dichloromethane and at 5° C. combined with a solution of 0.45 g (1.5 mmol) of 1-acetyl-3-(1-chloro-1-phenyl-methylidene)-2-indolinone in 10 ml of dichloromethane and then stirred for 3 hours at ambient temperature. After removal of the solvent in vacuo the residue is taken up in ethyl acetate/water. The organic phase is washed with water, dried and the solvent is eliminated in vacuo. Then the mixture is dissolved in 15 ml of methanol, combined with 3 ml of 1N sodium hydroxide solution, stirred for 3 hours at ambient temperature and diluted with water and ethyl acetate. The organic phase is dried and concentrated by evaporation. The residue is heated in ethyl acetate, cooled, then suction filtered and dried.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06855710B2
Source datasetuspto-grants-2005_02
ORD IDord-1b37d1a554874b21b6de10e259d2d9a6
Source noteuspto-grants-2005_02