참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Ethyl Acetate | HCID 8857 | — |
| 반응물 | 1,4-Dioxane | HCID 31275 | — |
| 반응물 | Ethyl 4-oxobutanoate | HCID 82395 | — |
| 반응물 | 4-(2-formyl-phenylethynyl)-N,N-dimethyl-benzenesulfonamide | HCID 59350855 | — |
| 촉매 | Gold tribromide | HCID 82525 | — |
| 생성물 | [4-(4-Dimethylsulfamoyl-benzoyl)-naphthalen-2-yl]-acetic acid ethyl ester | HCID 59350849 | 29% |
반응 단계
A suspension of gold(III) bromide (38 mg, 0.087 mmol), 4-oxo-butyric acid ethyl ester (377 mg, 2.9 mmol) and 4-(2-formyl-phenylethynyl)-N,N-dimethyl-benzenesulfonamide (454 mg, 1.45 mmol) in anhydrous dioxane (10 mL) was heated at 100° C. for 4 hours. After being cooled to room temperature, the mixture was treated with ethyl acetate, and then washed with water. The collected organic layer was dried over anhydrous sodium sulfate, filtered, and concentrated in vacuo. Flash chromatography (RediSep® Flash column, 230-400 mesh, 25-60% ethyl acetate in hexane) gave [4-(4-dimethylsulfamoyl-benzoyl)-naphthalen-2-yl]-acetic acid ethyl ester (180 mg, 29%). MS (ESI+) cald. for C23H23NO5S [(M+H)+] 425, obsd. 426.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08124629B2 |
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| 출처 데이터셋 | uspto-grants-2012_02 |
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| ORD ID | ord-5b350a69c57e4ada870ac98732ece1a2 |
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| 출처 메모 | uspto-grants-2012_02 |
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