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6-Methoxyquinoline → 5-Bromo-6-methoxyquinoline
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 6-Methoxyquinoline | HCID 14860 | — |
| 反応物 | Bromine | HCID 24408 | — |
| 反応物 | Sodium Bisulfite | HCID 23665763 | — |
| 溶媒 | Acetic Acid | HCID 176 | — |
| 生成物 | 5-Bromo-6-methoxyquinoline | HCID 18414128 | 58.7% |
反応手順
To a solution of 6-methoxyquinoline (5 g, 31.4 mmol) in acetic acid (50 mL) was slowly added Br2 neat (1.62 mL, 31.4 mmol). The reaction mixture was stirred at ambient temperature for 1 hour and then poured onto ice. Saturated aqueous sodium bisulfite was added, and the resulting slurry was extracted into EtOAc (2×200 mL). The organic fractions were combined, dried over Na2SO4, concentrated, and purified by column chromatography (5% MeOH/CH2Cl2) affording 4.39 g of the title compound as the acetate salt. The free base was prepared by washing the salt with 1 N NaOH (50 mL) and H2O (100 mL) and extracting into CH2Cl2 (200 mL). The organic fractions were concentrated affording 3.89 g (52%) of the title compound as a pink solid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06313126B1 |
| 出典データセット | uspto-grants-2001_11 |
| ORD ID | ord-04db3afc05d0439e8c9082b013422ddd |
| 出典メモ | uspto-grants-2001_11 |