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Pyridine → 1-Amino-2,4-di-n-dodecylaminoanthraquinone
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Pyridine | HCID 1049 | — |
| 反応物 | 1-Amino-2,4-dibromoanthraquinone | HCID 6681 | — |
| 反応物 | Dodecylamine | HCID 13583 | — |
| 反応物 | Potassium Acetate | HCID 517044 | — |
| 触媒 | Cupric acetate | HCID 8895 | — |
| 溶媒 | Benzene | HCID 241 | — |
| 生成物 | 1-Amino-2,4-di-n-dodecylaminoanthraquinone | HCID 21407063 | — |
反応手順
A reactor was charged with 19 g of 1-amino-2,4-dibromoanthraquinone, 28 g of dodecylamine, 0.4 g of copper acetate, 5 g of potassium acetate and 40 g of pyridine and the reaction was effected at an elevated temperature of 115°-120° C. for 20 hours under stirring. The reaction product was dissolved in benzene and insoluble matters were separated, followed by distillation of benzene and recrystallization from glacial acetic acid. A blue solid of 1-amino-2,4-di-n-dodecylaminoanthraquinone was obtained by the reaction of the following formula: ##STR8##
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04051052 |
| 出典データセット | uspto-grants-1977_09 |
| ORD ID | ord-475519ffedd541a484de268e39aa79e6 |
| 出典メモ | uspto-grants-1977_09 |