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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 5507Generated: October 26, 2026

4-Nitrophenol → 3-Ethyl-5-acrylamido-2-methylbenzoxazolium p-toluene sulfonate

https://huagongshe.com/reaction/5507

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-NitrophenolHCID 980—
ReactantEthyl p-methylbenzenesulfonateHCID 6638—
ReactantDimethylacetamideHCID 31374—
ReactantN-(2-Methylbenzo[d]oxazol-5-yl)acrylamideHCID 19796105—
SolventDiethyl EtherHCID 3283—
Product3-Ethyl-5-acrylamido-2-methylbenzoxazolium p-toluene sulfonateHCID 19796102—

Reaction Conditions

Temperature120 °C

Reaction Steps

About 100 parts of (3) are combined with about 109 parts of ethyl p-toluene sulfonate, 100 ml dimethylacetamide, and 5 ml p-nitrophenol (to inhibit polymerization) in a 500 ml three-necked flask equipped with a mechanical stirrer and condenser. The reaction mixture is heated at about 120° C. for about 5 hours while stirring under argon, then stirred at room temperature for about 15 hours, monitored using thin layer chromatography (TLC). After the reaction mixture is cooled to room temperature, it is poured into about 1500 ml of dry ethyl ether, decanted and stirred in fresh ethyl ether. The ethyl ether procedure is repeated until the oil product changes to a tacky solid which is then allowed to stand in ethyl ether overnight. The solid is filtered off and washed several times with butyronitrile to remove all starting material. The solid is washed further with ethyl ether and dried to yield 3-ethyl-5-acrylamido-2-methylbenzoxazolium p-toluene sulfonate (4) as a mustard-yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05244994
Source datasetuspto-grants-1993_09
ORD IDord-b701611ad3e041048caec74b4e9736d0
Source noteuspto-grants-1993_09