참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Cesium carbonate | HCID 10796 | — |
| 반응물 | 1,2-Ethanediol, 1,2-dimethanesulfonate | HCID 20796 | — |
| 반응물 | 2-Hydroxy-5-methoxybenzaldehyde | HCID 95695 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 5-Methoxy-2-(2-mesyloxyethoxy)-benzaldehyde | HCID 59765855 | 78% |
반응 단계
To a vigorously stirred solution of 15,2 g (100 mmol) 2-hydroxy-5-methoxy-benzaldehyde and 42.4 g (130 mmol) caesium carbonate in 350 ml DMF at 0° C. was added 27,3 g (125 mmol) 1,2-bis-methanesulfonyloxy-ethane ((J. Med. Chem.; 47; 17; (2004); 4300-4315) in 50 ml DMF dropwisely. The reaction mixture was stirred vigorously at 70° C. for 5 h. The solvent was evaporated. 200 ml water and 200 ml ethyl acetate were added. The organic phase was separated. The aqueous phase was extracted three times with 100 ml ethyl acetate each. The combined organic phases were washed with 50 ml water and 50 ml brine. The organic phase was dried with magnesium sulfate and evaporated. The crude product was purified by silica column chromatography (gradient ethylacetate:hexane 1:6, ethyl acetate→1:2). The desired product 4a was obtained in 78% yield (21.4 g, 78 mmol) as yellow oil.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07803960B2 |
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| 출처 데이터셋 | uspto-grants-2010_09 |
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| ORD ID | ord-3d753c14c9994b67aa656b2412c7b636 |
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| 출처 메모 | uspto-grants-2010_09 |
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