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4-Hydroxy-3-nitrobenzoic acid → Benzoic acid, 4-hydroxy-3-nitro-, methyl ester
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 4-Hydroxy-3-nitrobenzoic acid | HCID 12033 | — |
| 反応物 | Trimethylsilyldiazomethane | HCID 167693 | — |
| 溶媒 | Benzene methanol | HCID 21927730 | — |
| 生成物 | Benzoic acid, 4-hydroxy-3-nitro-, methyl ester | HCID 66835 | 75.2% |
反応手順
To a stirred solution of 4-hydroxy-3-nitrobenzoic acid (5.18 g, 28.29 mmol) in benzene-MeOH (4:1, v/v, 140 mL) was added TMSCHN2 (14.10 mL, 28.20 mmol, 2 M solution in hexane) at room temp, and the resulting mixture was stirred overnight. The mixture was evaporated and the residue was purified by column chromatography on silica-gel with CHCl3 as eluent to give 4.18 g (75%) methyl 3-nitro-4-hydroxybenzoate as a yellow crystalline solid. 1H-NMR (CDCl3) d 3.95 (s, 3H), 7.22 (d, 1H, J=8.8 Hz), 8.24 (dd, 1, J=2.0, 8.8 Hz), 8.83 (d, 1H, J=2.0 Hz), 10.89 (s, 1H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06756378B2 |
| 出典データセット | uspto-grants-2004_06 |
| ORD ID | ord-c59c423fd790488d8f470cc71dbddfd2 |
| 出典メモ | uspto-grants-2004_06 |