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Dichloromethane → 3-Nitro-5-(octadecyloxy)benzoic acid methyl ester
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Dichloromethane | HCID 6344 | — |
| 反応物 | 1-Bromooctadecane | HCID 8218 | — |
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | Methyl 3-hydroxy-5-nitrobenzoate | HCID 239344 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | 3-Nitro-5-(octadecyloxy)benzoic acid methyl ester | HCID 53698954 | 92.3% |
反応手順
A mixture of 1.7 g (8.6 mmol) of 3-hydroxy-5-nitrobenzoic acid methyl ester [prepared as described by D. J. Abraham, D. M. Gazze, P. E. Kennedy and M. Mokotoff, J. Med. Chem. 27, 1549 (1984], 3.2 g (9.5 mmol) of 1-bromooctadecane and 1.8 g (12.9 mmol) of potassium carbonate in 35 ml of anhydrous DMF was stirred and heated at 75° for 25 hours. After cooling, 150 ml of methylene chloride was added and the insoluble salts were removed by filtration. The filtrate was concentrated at reduced pressure to a solid which was purified by HPLC using 30% methylene chloride-hexane to give 3.57 g (92% yield, mp 64°-66°) of 3-nitro-5-(octadecyloxy)benzoic acid methyl ester.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05324747 |
| 出典データセット | uspto-grants-1994_06 |
| ORD ID | ord-1a827c1e879a4dd9a9c65dc5ebaf5607 |
| 出典メモ | uspto-grants-1994_06 |