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HRID 53267作成日:2026年10月25日

p-Toluenesulfonic acid → t-Butylphenol 2-Phenyl-2-oxazoline

https://huagongshe.com/reaction/53267

反応式

関与物質

役割名称HCID仕込み量
反応物p-Toluenesulfonic acidHCID 6101—
反応物2-Tert-ButylphenolHCID 6923—
反応物2-Phenyl-2-oxazolineHCID 244030—
溶媒TetrahydrofuranHCID 8028—
生成物t-Butylphenol 2-Phenyl-2-oxazolineHCID 86750688—

反応条件

温度170 °C

反応手順

A pure sample of the addition product of t-butylphenol and 2-phenyl-2-oxazoline was obtained for comparative purposes as follows: in a side-armed test tube, 2.94 grams 2-phenyl-2-oxazoline and 3.00 grams t-butyl phenol were combined with 0.08 gram pTSA. The stirred mixture was heated under nitrogen at 170° C. for 16 hours. Pure amide ether addition product [B] was obtained from the reaction mixture by column chromatography on silica gel. The crude reaction mixture was taken up in tetrahydrofuran and introduced onto the column, which was subsequently eluted with 1/1 (v/v) hexane/ethyl acetate. Desired fractions were identified by thin layer chromatography, and the product structure was confirmed by 1H and 13C NMR. The reaction is outlined in Scheme 1. ##STR3##

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05618896
出典データセットuspto-grants-1997_04
ORD IDord-6b81bcb965514342b8020cef002faef9
出典メモuspto-grants-1997_04