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3-Hydroxybenzaldehyde → 3-(2-Bromoethoxy)benzaldehyde
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 3-Hydroxybenzaldehyde | HCID 101 | — |
| 反応物 | Acetonitrile | HCID 6342 | — |
| 反応物 | 1,1-Dibromoethane | HCID 11201 | — |
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 溶媒 | Diethyl Ether | HCID 3283 | — |
| 生成物 | 3-(2-Bromoethoxy)benzaldehyde | HCID 2735565 | — |
反応手順
A mixture of 3-hydroxybenzaldehyde (5.17 g, 42.33 mmol), K2CO3 (58.5 g) and CH3CN (100 ml) was stirred at room temperature for 15 minutes, then dibromoethane (18.3 ml) was added. The reaction mixture was stirred at room temperature for 30 minutes, then at reflux for 3-4 hours. Additional dibromoethane was added and then the reaction mixture was refluxed overnight. The reaction mixture was cooled, filtered, and the filtrate was stripped to afford an oil. The oil was dissolved in ether (300 ml), washed with 5N NaOH (2×75 ml) and the ether layer was dried over MgSO4 and stripped. The residue was purified by column chromatography on silica gel eluting with 10% ethyl acetate/hexane to afford 5.23 g of 3-(2-bromoethoxy)benzaldehyde.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05958929 |
| 出典データセット | uspto-grants-1999_09 |
| ORD ID | ord-906f685a24c447c887bf4cd3a385dd1f |
| 出典メモ | uspto-grants-1999_09 |