関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Methanol | HCID 887 | — |
| 反応物 | 2,6-Dimethylbenzoic acid | HCID 12439 | — |
| 反応物 | 2,6-Dimethyl-3-nitrobenzoic acid | HCID 239329 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 2,6-Dimethyl-3-nitrobenzoic acid | HCID 239329 | — |
| 生成物 | (2,6-Dimethyl-3-nitrophenyl)methanol | HCID 10487641 | 88.3% |
反応手順
2,6-Dimethyl-3-nitrobenzoic acid was prepared by nitrating 2,6-dimethylbenzoic acid. A solution of 2,6-dimethyl-3-nitrobenzoic acid (30 grams, 0.15 mole) in tetrahydrofuran (100 ml) was stirred under nitrogen. Borane-methyl sulfide complex (20 ml, 0.2 mole) was added dropwise at room temperature. When one fourth of the borane complex had been added the reaction mixture was brought to reflux. Reflux continued for one hour after complete addition of the borane complex. The reaction mixture was cooled to 0°, and cold methanol (500 ml) was added dropwise until foaming ceased and then added rapidly. The solvent was evaporated, and the crude product was dissolved in methylene chloride and washed with 2 N sodium hydroxide. The solvent was removed by evaporation to give (2,6-dimethyl-3-nitrophenyl)methanol (12.0 grams; mp 84°-92°).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04375476 |
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| 出典データセット | uspto-grants-1983_03 |
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| ORD ID | ord-de9954a06a1e436db4426b380dac932f |
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| 出典メモ | uspto-grants-1983_03 |
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