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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2414762Generated: November 2, 2026

4-Nitroaniline → HCID 69202260, compound

https://huagongshe.com/reaction/2414762

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-NitroanilineHCID 7475—
Reactant4-Nitroanilinium chlorideHCID 85156—
ReactantEthyl 3-(3-fluorophenyl)-3-oxopropanoateHCID 2063904—
Solvent1-ButanolHCID 263—
ProductHCID 69202260HCID 6920226020.8%

Reaction Conditions

Temperature118 °C

Reaction Steps

3-(3-Fluorophenyl)-3-oxo-propionic acid ethyl ester, 106.3 grams (0.506 moles), 4-nitro-aniline, 63.0 grams (0.456 moles), and 4-nitro-aniline hydrochloride 4.0 grams (0.023 moles) were placed in a dry 2 L round-bottom flask. To the mixture was added 1.3 L of n-butanol, the flask was fitted with a Soxhlet extractor (cup volume of 0.3 L), condenser and nitrogen inlet. Dry, activated 4 Å sieves (200 grams) were placed in the extractor cup and the reaction mixture heated to reflux at 118° C. under nitrogen and maintained at that temperature for 90 hours. The reaction mixture was decanted while hot from a small amount of solids and chilled to −15° C. for 48 hours Crystalline solids were collected by vacuum filtration. The crystals were washed with 0.2 L of cold ethanol and two 0.2 L portions of hexanes and vacuum dried at 50° C. overnight to yield 35.8 grams (20.8% yield) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06815447B2
Source datasetuspto-grants-2004_11
ORD IDord-81cb8f7f8f6a4122ae8e19113514e362
Source noteuspto-grants-2004_11