Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 68211Generated: October 29, 2026

Ammonium Chloride → 4-Hydroxyphenyl 10-methylacridan-9-carboxvlate

https://huagongshe.com/reaction/68211

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant4-(Tert-butyldimethylsilyloxy)phenyl 10-methylacridinium-9-carboxylate trifluoromethanesulfonateHCID 86615371—
CatalystZincHCID 23994—
SolventEthanolHCID 702—
SolventDichloromethaneHCID 6344—
Product4-Hydroxyphenyl 10-methylacridan-9-carboxvlateHCID 54418877—

Reaction Steps

Into a 50 mL round bottom flask equipped with magnetic stirrer, reflux condensor and heating mantle under an argon atmosphere was charged a solution of 1.42 parts of the 4-(tert-butyldimethylsilyloxy)phenyl 10-methylacridinium-9-carboxylate trifluoromethanesulfonate in 200 mL of ethanol. Then 16 arts NH4Cl was added in five portions, followed by 19.3 parts of Zn in five portions to a hot yellow solutions causing immediate decolorization of the solution. The reaction mixture was refluxed for 2 hrs and filtered. The solid was washed with 2×25 mL of ethanol. The combined filtrate was concentrated under reduced pressure to give off-white solid. The solid was dissolved in 250 mL of dichloromethane and washed with 100 mL of deionized water. After separation the organic layer was dried over anhydrous Na2SO4 and filtered. The solution was concentrated under reduced pressure and purified by column chromatography on silica gel with 10% ethyl acetate-hexane to yield 0.76 parts of 4-Hydroxyphenyl 10-methylacridan-9-carboxylate. The structure was confirmed as:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08822233B2
Source datasetuspto-grants-2014_09
ORD IDord-883438eaf170468d9b832713eadcafcc
Source noteuspto-grants-2014_09