HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 24729Generated: October 26, 2026
P-Anisidine → HCID 178492232, compound
https://huagongshe.com/reaction/24729
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | P-Anisidine | HCID 7732 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-Acetyl-3-(1-chloro-1-phenyl-methylidene)-2-indolinone | HCID 69743657 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178492232 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06855710B2 |
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| Source dataset | uspto-grants-2005_02 |
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| ORD ID | ord-1b37d1a554874b21b6de10e259d2d9a6 |
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| Source note | uspto-grants-2005_02 |
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