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HRID 5507作成日:2026年10月24日

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

https://huagongshe.com/ja/reaction/5507

反応式

関与物質

役割名称HCID仕込み量
反応物4-NitrophenolHCID 980—
反応物Ethyl p-methylbenzenesulfonateHCID 6638—
反応物DimethylacetamideHCID 31374—
反応物N-(2-Methylbenzo[d]oxazol-5-yl)acrylamideHCID 19796105—
溶媒Diethyl EtherHCID 3283—
生成物3-Ethyl-5-acrylamido-2-methylbenzoxazolium p-toluene sulfonateHCID 19796102—

反応条件

温度120 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05244994
出典データセットuspto-grants-1993_09
ORD IDord-b701611ad3e041048caec74b4e9736d0
出典メモuspto-grants-1993_09