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Acetamide → 3,5-Dihydroxy-4-phenylazo-benzoic acid methyl ester
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Acetamide | HCID 178 | — |
| 反応物 | Bromine | HCID 24408 | — |
| 反応物 | Bromosuccinimide | HCID 38309 | — |
| 反応物 | 3-Hydroxy-5-keto-4-phenylazo-3-cyclohexenecarboxylic acid methyl ester | HCID 136056374 | — |
| 溶媒 | Chloroform | HCID 6212 | — |
| 生成物 | 3,5-Dihydroxy-4-phenylazo-benzoic acid methyl ester | HCID 136059786 | — |
反応手順
54.8 G. of 3-hydroxy-5-keto-4-phenylazo-3-cyclohexene-carboxylic acid methyl ester, 12.0 g. of acetamide and 2.0 g. of bromosuccinimide were stirred in 600 ml. of chloroform and treated dropwise with 32.0 g. of bromine dissolved in 400 ml. of chloroform. The reaction temperature was kept below 35° C. Separation of acetamide hydrobromide soon began. The mixture was stirred at room temperature for an additional 30 minutes and the acetamide hydrobromide was removed by filtration. The filtrate was evaporated to dryness and the residue taken up in a small amount of ethanol, removed by filtration under vacuum and washed with ethanol, whereby there was obtained 3,5-dihydroxy-4-phenylazo-benzoic acid methyl ester of melting point 216°-218° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04076810 |
| 出典データセット | uspto-grants-1978_02 |
| ORD ID | ord-42277452546140d19318f86d2fa18867 |
| 出典メモ | uspto-grants-1978_02 |