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HRID 53267생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/53267

반응식

참여 물질

역할이름HCID투입량
반응물p-Toluenesulfonic acidHCID 6101—
반응물2-Tert-ButylphenolHCID 6923—
반응물2-Phenyl-2-oxazolineHCID 244030—
용매TetrahydrofuranHCID 8028—
생성물t-Butylphenol 2-Phenyl-2-oxazolineHCID 86750688—

반응 조건

온도170 °C

반응 단계

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##

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05618896
출처 데이터셋uspto-grants-1997_04
ORD IDord-6b81bcb965514342b8020cef002faef9
출처 메모uspto-grants-1997_04