化工社化工社 化学情報印刷レポート · 研究参考用
Hydrochloric Acid → Ethyl 3-(4-carboxy-2-methylphenylhydrazono)-4-oxopentanoate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | 4-Amino-3-methylbenzoic acid | HCID 75598 | — |
| 反応物 | Ethyl 3-acetyl-4-oxopentanoate | HCID 87820 | — |
| 反応物 | Sodium Nitrite | HCID 23668193 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | Pyridine | HCID 1049 | — |
| 生成物 | Ethyl 3-(4-carboxy-2-methylphenylhydrazono)-4-oxopentanoate | HCID 86751496 | — |
反応手順
A mixture of 3 g. (19.8 mmol) of 4-amino-3-methylbenzoic acid in 50 ml. of water and 50 ml. of ethanol and 3.56 ml. of concentrated hydrochloric acid was cooled in an ice bath and then 1.5 g. of NaNO2 (21.8 mmol.) in 10 ml. of water was added portionwise. The mixture was allowed to come to room temperature and then added to a solution of 4.06 g. (21.8 mmol.) of ethyl 3-acetyl-4-oxopentanoate and 8 ml. of pyridine in 25 ml. of ethanol. The reaction mixture was left for 24 hours at room temperature with stirring. The mixture was acidified with concentrated hydrochloric acid and diluted with 20 ml. of water. The resulting solid was collected and washed with water and pentane to yield 5.2 g.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05821243 |
| 出典データセット | uspto-grants-1998_10 |
| ORD ID | ord-5b68ae39fb0d454b819718511809b210 |
| 出典メモ | uspto-grants-1998_10 |