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Ammonium Hydroxide → 6-(Difluoromethoxy)-1,3-benzothiazol-2-amine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Ammonium Hydroxide | HCID 14923 | — |
| 反応物 | Bromine | HCID 24408 | — |
| 反応物 | Potassium thiocyanate | HCID 516872 | — |
| 反応物 | 4-(Difluoromethoxy)aniline | HCID 737363 | — |
| 溶媒 | Acetic Acid | HCID 176 | — |
| 生成物 | 6-(Difluoromethoxy)-1,3-benzothiazol-2-amine | HCID 19585898 | 87.3% |
反応手順
To 4-(difluoromethoxy)aniline (9.55 g, 60 mmol) in acetic acid (90 mL) was added potassium thiocyanate (KSCN) (12.41 mL, 240 mmol). The mixture was stirred for 20 minutes (KSCN dissolved into solution). To this mixture bromine (3.08 mL, 60.0 mmol) in acetic acid (40 mL) was added dropwise over 20 minutes. The reaction was stirred at room temperature overnight. It was poured into a mixture of 800 ml ice water and 200 ml saturated ammonium hydroxide. The product was extracted with ethyl acetate (5×). The organics were combined, washed with brine, dried over sodium sulfate, filtered and concentrated in vacuo to afford 6-(difluoromethoxy)benzo[d]thiazol-2-amine (12.6 g, 52.4 mmol, 87% yield) as a yellow solid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07863291B2 |
| 出典データセット | uspto-grants-2011_01 |
| ORD ID | ord-8c8c3eff73804232af6b26a08d8f76c1 |
| 出典メモ | uspto-grants-2011_01 |