関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Benzene | HCID 241 | — |
| 反応物 | Hydrogen Bromide | HCID 260 | — |
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | 8-Hydroxyquinoline | HCID 1923 | — |
| 反応物 | Aluminum bromide | HCID 24409 | — |
| 生成物 | Ijrzsljquollsz-uhfffaoysa- | HCID 12036201 | — |
反応手順
To a stirred suspension of AlBr3 (4.80 g, 18 mmol) in benzene (4.8 mL, 55 mmol) was added 8-hydroxyquinoline (0.50 g, 3.4 mmol). The resulting mixture was saturated with HBr (g) and then stirred at 40° C. for 48 h. The reaction mixture was cooled to ambient temperature and poured onto ice (50 g). The resulting mixture was adjusted to pH=1-2 by addition of concentrated HCl and then was extracted with EtOAc (3×20 mL), discarding the organic extracts. The aqueous layer was adjusted to pH 12 by addition of NaOH (s), keeping the temperature below 10° C., and was then extracted with EtOAc (3×20 mL). These combined organic extracts were washed with brine (30 mL), dried over sodium sulfate, filtered, and concentrated in vacuo to give the title compound in sufficient purity for use in the next step. MS: m/z=223.8 (M+1).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US09227973B2 |
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| 出典データセット | uspto-grants-2016_01 |
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| ORD ID | ord-c51cf7a87f24409c9eca2cbe59d0345b |
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| 出典メモ | uspto-grants-2016_01 |
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