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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2396061Generated: October 30, 2026

Acetic Acid → HCID 10320817, compound

https://huagongshe.com/reaction/2396061

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantAnilineHCID 6115—
ReactantP-AnisidineHCID 7732—
Reactant4,5-Bis(trimethylsilyloxy)cyclohexa-1,4-diene-1,2-dicarboxylic acid dimethyl esterHCID 10022190—
ProductHCID 10320817HCID 10320817—

Reaction Steps

A solution of 4.8 g (12 mmol) 4,5-Bis(trimethylsilyloxy)-cyclohexa-1,4-diene-1,2-dicarboxylic acid dimethyl ester (Example 1a), 2.6 g (24 mmol) p-anisidine and 2.2 ml (24 mmol) aniline in 48 ml of glacial acetic acid is boiled under reflux for 2hours. The reaction mixture is cooled, the solvent is evaporated and the dark-brown residue is dissolved in ethyl acetate and the solution is washed in succession with 40 ml of 1N HCl, 100 ml of saturated NaHCO3and twice with water, dried with magnesium sulfate and concentrated by evaporation. The evaporation residue is chromatographed on silica gel withethyl acetate/hexane 1:3 and the product fractions are concentrated by evaporation. This way, in the first product fractions 4,5-bis-(4-methoxy-anilino)-phthalic acid dimethyl ester is obtained in the form of a yellow foam: FAB-MS: 437 [M+ +H]. The evaporation residue of the product fractions following thereafter is recrystallized, and 4-anilino-5-(4-methoxy-anilino)-phthalic acid dimethyl ester is obtained in the form of yellow crystals, m.p. 122°-4° C., FAB-MS: 407 [M+ +H].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05491144
Source datasetuspto-grants-1996_02
ORD IDord-77722b88c8c2460ca96a30ca52c475cd
Source noteuspto-grants-1996_02