Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 226159생성일: 2026년 10월 25일
Sodium Bicarbonate → 3-{3-[(E)-2-Phenylethenesulfonylamino]phenyl}acrylic acid methyl ester
https://huagongshe.com/reaction/226159
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Sodium Bicarbonate | HCID 516892 | — |
| 반응물 | (E)-2-phenylethene-1-sulfonyl chloride | HCID 5369377 | — |
| 반응물 | Methyl 3-aminocinnamate | HCID 54385173 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | 1,4-Dioxane | HCID 31275 | — |
| 생성물 | 3-{3-[(E)-2-Phenylethenesulfonylamino]phenyl}acrylic acid methyl ester | HCID 67019599 | 70.2% |
반응 단계
A solution of (E)-2-phenylethenesulfonyl chloride (24a) (0.59 g, 2.82 mmol) in dioxane (3 ml) was added to a mixture of 3-(3-aminophenyl)-acrylic acid methyl ester (23) (0.50 g, 2.82 mmol) in dioxane (12 ml) and NaHCO3 (0.36 g, 4.28 mmol) in water (8 ml), and the resultant solution was stirred at room temperature until the completion of the reaction (control by TLC). The reaction mixture was evaporated and the residue was partitioned between ethyl acetate and 2N HCl. The organic layer was washed successively with water, saturated NaCl, and dried (Na2SO4). The solvent was removed and the residue was chromatographed on silica gel with chloroform-ethyl acetate (100:2, v/v) as eluent to give the title compound (0.68 g, 70%) as a white solid. 1H NMR (CDCl3, HMDSO), δ: 3.78 (3H, s); 6.39 (1H, d, J=16.0 Hz); 6.77 (1H, d, J=15.8 Hz); 6.78 (1H, s); 7.17-7.48 (9H, m); 7.49 (1H, d, J=15.8 Hz); 7.58 (1H, d, J=16.0 Hz).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07557140B2 |
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| 출처 데이터셋 | uspto-grants-2009_07 |
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| ORD ID | ord-794ff716d7644b8a9501b4c7092df5f9 |
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| 출처 메모 | uspto-grants-2009_07 |
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