HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2396047Generated: October 30, 2026
4-Benzyloxyaniline → HCID 21753024, compound
https://huagongshe.com/reaction/2396047
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Benzyloxyaniline | HCID 22860 | — |
| Reactant | HCID 10022190 | HCID 10022190 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 21753024 | HCID 21753024 | — |
Reaction Steps
A solution of 2.4 g (6 mmol) of 4,5-bis(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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05491144 |
|---|
| Source dataset | uspto-grants-1996_02 |
|---|
| ORD ID | ord-22316e67bd4445d09e23b80e71c6999c |
|---|
| Source note | uspto-grants-1996_02 |
|---|