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Benzyl Bromide → 2-(Benzyloxy)-3-methoxybenzaldehyde
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Benzyl Bromide | HCID 7498 | — |
| 反応物 | o-Vanillin | HCID 8991 | — |
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | 2-(Benzyloxy)-3-methoxybenzaldehyde | HCID 1268087 | 93% |
反応手順
A mixture of 196.0 g (1.30 mole) of o-vanillin (Aldrich), 200 g of benzyl bromide (Aldrich), 500 g of anhydrous potassium carbonate and 1,500 mL of absolute ethanol is heated, with stirring, at reflux for 6 hours. After cooling, the supernatant is decanted and the remainder is filtered. The combined filtrate and supernatant is concentrated at reduced pressure to remove solvent. The remaining oil is extracted into 1 L of ether. The ether solution is washed with 500 mL of water, 600 mL of 1% potassium hydroxide solution, and 500 mL of water and then dried (potassium carbonate) and concentrated to give 263.4 g (84% yield) of product; mp 41°-43° C. Reported mp, 43° C. (Chem. Abstr. 62:16110a).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05246943 |
| 出典データセット | uspto-grants-1993_09 |
| ORD ID | ord-0b20c9191db0436d9a89e14bbc14aaef |
| 出典メモ | uspto-grants-1993_09 |