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Sulfuric Acid → Methyl 5-Iodosalicylate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Sulfuric Acid | HCID 1118 | — |
| 反応物 | 5-Iodosalicylic acid | HCID 8388 | — |
| 反応物 | Trimethyl orthoformate | HCID 9005 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | Methyl 5-Iodosalicylate | HCID 248910 | — |
反応手順
5-Iodosalicylic acid (Aldrich Chemical Company, Milwaukee, Wis.) is converted to the methyl ester by reaction with methanol, trimethyl orthoformate and sulfuric acid. The 5-iodosalicylic acid methyl ester thus obtained is reacted with (trimethylsilyl)acetylene (Aldrich Chemical Company, Milwaukee, Wis.) in the presence of palladium. The trimethylsilyl group is removed and two equivalents of the resultant 5-acetylenylsalicylic acid methyl ester is reacted with 4,4'-dibromobiphenyl (Aldrich Chemical Company, Milwaukee, Wis.) in the presence of palladium as above. The resultant alkynyl analogue of Chrysamine G, 4,4'-bis(3-methoxycarbonyl-4-hydroxyphenylacetylenyl)-biphenyl is prepared by hydrolysis of the ester as described above.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06133259 |
| 出典データセット | uspto-grants-2000_10 |
| ORD ID | ord-41e292c8f77545939f90e40c8d409a74 |
| 出典メモ | uspto-grants-2000_10 |