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2-Bromo-1-(4-hydroxyphenyl)ethanone → 4'-Hydroxyacetophenone
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 2-Bromo-1-(4-hydroxyphenyl)ethanone | HCID 4964 | — |
| 反応物 | 1-(2-Morpholin-4-ylethyl)-2-aminobenzimidazole | HCID 568011 | — |
| 溶媒 | Chloroform | HCID 6212 | — |
| 溶媒 | Ethyl Acetate | HCID 8857 | — |
| 生成物 | 4'-Hydroxyacetophenone | HCID 7469 | — |
反応手順
A mixture of 2-amino-1-(2-morpholinoethyl) benzimidazole (10 mmol, 2.46 g) and 4-hydroxyphenacyl bromide (10 mmol, 2.15 g) (obtained by bromination of para-hydroxyacetophenone with cupric bromide in a mixture of chloroform and ethyl acetate) is heated at reflux for 1 hour in 10 ml of dimethylformamide. After cooling, the mixture is poured into 50 ml of water and rendered alkaline with ammonium hydroxide. The resulting oil is removed and treated with water. The crystallised residue is filtered, dried, and recrystallised from ethanol.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05623073 |
| 出典データセット | uspto-grants-1997_04 |
| ORD ID | ord-256fd092d78a4b3982d8846e0ae85ff0 |
| 出典メモ | uspto-grants-1997_04 |