関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Acetic Acid | HCID 176 | — |
| 反応物 | Hydrogen Bromide | HCID 260 | — |
| 反応物 | 2,6-Dichloro-2',3',4'-trimethoxy-6'-methyl-benzophenone | HCID 22719953 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | 2,6-Dichloro-2',3'-dihydroxy-4'-methoxy-6'-methyl-benzophenone | HCID 54569551 | — |
反応手順
A mixture of 2,6-dichloro-2',3',4'-trimethoxy-6'-methyl-benzophenone (1.78 g; 5 mmol) hydrobromic acid (7.5 ml; 30% in acetic acid) and acetic acid (7.5 ml) is stirred at 75° C. for 2 hours. Water is added and the mixture extracted with methylenechloride. The extract is washed with waterand shaken with 2N sodium hydroxide. The alcaline solution is acidified with hydrochloric acid, the separated compound dissolved in methylenechloride and the solution washed with water. After evaporation ofthe solvent purification is carried out by chromatography (flash column, filled with 36 g of silicagel; elution with 500 ml of petrolether/ethylacetate (4:1; v/v) and 250 ml of petrolether/ethylacetate(1:1; v/v)). the fraction containing the compound is concentrated, the compound crystallized. The yellow crystals are washed with petrolether andsucked off; 0.64 g (39% y), mp. 182° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05866722 |
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| 出典データセット | uspto-grants-1999_02 |
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| ORD ID | ord-f2bc4d1e56aa4859abea606d965acb6e |
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| 出典メモ | uspto-grants-1999_02 |
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