Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1787249생성일: 2026년 10월 26일
p-Toluenesulfonic acid monohydrate → N-(3-(4-Isopropylphenyl)-4,6-dimethyl-7-vinyl-2,3-dihydro-1-benzofuran-5-yl)-3,3-dimethylbutanamide
https://huagongshe.com/reaction/1787249
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| 반응물 | N-(7-(1-hydroxyethyl)-3-(4-isopropylphenyl)-4,6-dimethyl-2,3-dihydro-1-benzofuran-5-yl)-3,3-dimethylbutanamide | HCID 23113921 | — |
| 용매 | Toluene | HCID 1140 | — |
| 생성물 | N-(3-(4-Isopropylphenyl)-4,6-dimethyl-7-vinyl-2,3-dihydro-1-benzofuran-5-yl)-3,3-dimethylbutanamide | HCID 23113980 | 89% |
반응 단계
A solution of N-(7-(1-hydroxyethyl)-3-(4-isopropylphenyl)-4,6-dimethyl-2,3-dihydro-1-benzofuran-5-yl)-3,3-dimethylbutanamide (1.23 g, 3.02 mmol) obtained in Example 22 and p-toluenesulfonic acid monohydrate (20 mg) in toluene (20 mL) was refluxed with heating at 80° C. for 1 hour under an argon atmosphere. The reaction solution was washed with an aqueous saturated sodium hydrogen carbonate solution, dried over magnesium sulfate, and concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (ethyl acetate:hexane=1:9) to obtain 1.09 g (yield: 89%) of the title compound. Melting point: 171-172° C. (hexane-ethyl acetate).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07507841B2 |
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| 출처 데이터셋 | uspto-grants-2009_03 |
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| ORD ID | ord-1d62f685675d4844acf435735c109172 |
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| 출처 메모 | uspto-grants-2009_03 |
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