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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1376761Generated: November 1, 2026

4-Benzyloxyaniline → HCID 21753024, compound

https://huagongshe.com/reaction/1376761

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-BenzyloxyanilineHCID 22860—
ReactantHCID 12405273HCID 12405273—
SolventAcetic AcidHCID 176—
ProductHCID 21753024HCID 21753024—

Reaction Steps

A solution of 2.4 g (6 mmol) of 4,5-his (trimethylsilyloxy)cyclohexa-1,4-diene-1,2-dicarboxylic acid dimethyl ester (Example 1a) and 4.8 g (24 mmol) of 4-benzyloxyaniline in 24 ml of glacial acetic acid is boiled under reflux for 2 hours. The reaction mixture is cooled, the solvent is evaporated off and the dark-brown residue is dissolved in dichloromethane and the solution is washed in succession with 20 ml of 1N HCl, 50 ml of saturated NaHCO3 and twice with 20 ml of water, dried with sodium sulfate and concentrated by evaporation. The evaporation residue is dissolved while hot in ethyl acetate and filtered, then allowed to crystallize at 0°. The crystalline residue is chromatographed on silica gel with ethyl acetate/hexane 3:2 and the product fractions are concentrated by evaporation and recrystallized from ethyl acetate/hexane, yielding the title compound in the form of beige crystals, FAB-MS: 589 [M+ +H].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05663336
Source datasetuspto-grants-1997_09
ORD IDord-9ec0a892a682485383af2ab75b1f2fd6
Source noteuspto-grants-1997_09