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p-Toluenesulfonic acid → 6-Methoxy-2-(4-nitrophenyl) benzothiazole
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | p-Toluenesulfonic acid | HCID 6101 | — |
| 反応物 | 4-Nitrobenzoyl chloride | HCID 8502 | — |
| 反応物 | 2-Amino-5-methoxybenzene-1-thiol | HCID 235509 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 生成物 | 6-Methoxy-2-(4-nitrophenyl) benzothiazole | HCID 10660852 | 76% |
反応手順
A mixture of 2-amino-5-methoxybenzenethiol (5.0 g, 32.2 mmol) and 4-nitrobenzoyl chloride (6.0 g, 32.2 mmol) in toluene (250 ml) was heated under reflux with a catalytic amount of 4-toluenesulphonic acid in a Dean-Stark trap for 6 h. On cooling to room temperature the precipitate was collected by filtration, washed with toluene and recrystallised from AcOH to give the title compound (7.0 g, 76%) as a pale yellow solid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08895313B2 |
| 出典データセット | uspto-grants-2014_11 |
| ORD ID | ord-848e7a26756a46558dcb5d9f1baf8bc7 |
| 出典メモ | uspto-grants-2014_11 |