참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | p-Toluenesulfonic acid | HCID 6101 | — |
| 반응물 | 2-Tert-Butylphenol | HCID 6923 | — |
| 반응물 | 2-Phenyl-2-oxazoline | HCID 244030 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | t-Butylphenol 2-Phenyl-2-oxazoline | HCID 86750688 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05618896 |
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| 출처 데이터셋 | uspto-grants-1997_04 |
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| ORD ID | ord-6b81bcb965514342b8020cef002faef9 |
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| 출처 메모 | uspto-grants-1997_04 |
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