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N,N-Dimethylaniline → 6-Chloro-2-[(3-chloro-4-methoxyphenyl)amino]-3-nitrobenzoic acid
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | N,N-Dimethylaniline | HCID 949 | — |
| 反応物 | 3-Chloro-4-methoxyaniline | HCID 21441 | — |
| 反応物 | 2,6-Dichloro-3-nitrobenzoic acid | HCID 350623 | — |
| 溶媒 | Chloroform | HCID 6212 | — |
| 生成物 | 6-Chloro-2-[(3-chloro-4-methoxyphenyl)amino]-3-nitrobenzoic acid | HCID 13588347 | — |
反応手順
A mixture of 30 g of 3-chloro-4-methoxyaniline, 18.9 g of 2,6-dichloro-3-nitrobenzoic acid, and 150 ml N,N-dimethylaniline was heated at 100° under nitrogen for 24 hours. The reaction mixture was dissolved in chloroform and washed with dilute ammonium hydroxide. After the aqueous layer was washed with chloroform, it was acidified and the resulting orange solid was collected to provide 6-chloro-2[(3-chloro-4-methoxyphenyl)amino]-3-nitrobenzoic acid, mp 222°-228° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04588730 |
| 出典データセット | uspto-grants-1986_05 |
| ORD ID | ord-2b9a38beeb7c47feb5cac4c6de898dbd |
| 出典メモ | uspto-grants-1986_05 |