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3,4-Diaminobenzoic acid → 2,3-Bis(4-methoxyphenyl)quinoxaline-6-carboxylic acid
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 3,4-Diaminobenzoic acid | HCID 69263 | — |
| 反応物 | 4,4'-Dimethoxybenzil | HCID 71043 | — |
| 反応物 | 2,3-Bis(3-amino-4-hydroxyphenyl)quinoxaline-6-carboxylic acid dihydrochloride | HCID 136388340 | — |
| 生成物 | 2,3-Bis(4-methoxyphenyl)quinoxaline-6-carboxylic acid | HCID 980312 | — |
反応手順
Briefly, the AB2 monomer, 2,3-bis(3-amino-4-hydroxyphenyl)quinoxaline-6-carboxylic acid dihydrochloride, is synthesized by condensing 3,4-diaminobenzoic acid and 4,4′-dimethoxybenzil to afford 2,3-bis(4-methoxyphenyl) quinoxaline-6-carboxylic acid, followed by demethylation in hydrobromic acid in acetic acid to form 2,3-bis(4-hydroxyphenyl) quinoxaline-6-carboxylic acid. The latter is then nitrated using nitric acid (70% conc.) in acetic acid at room temperature, yielding 2,3-bis(3-nitro-4-hydroxyphenyl) quinoxaline-6-carboxylic acid. The desired monomer is prepared by catalytic reduction in the presence of palladium catalyst in 10% hydrochloric acid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06608171B1 |
| 出典データセット | uspto-grants-2003_08 |
| ORD ID | ord-b173923705b04832a408af0aacc722cf |
| 出典メモ | uspto-grants-2003_08 |