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HRID 66327作成日:2026年10月26日
1-Naphthalenesulfonic acid, 4-amino-5-hydroxy- → 5-Hydroxy-4-m-nitrobenzamido-1-naphthalenesulfonic acid sodium salt
https://huagongshe.com/reaction/66327
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 1-Naphthalenesulfonic acid, 4-amino-5-hydroxy- | HCID 6752 | — |
| 反応物 | Benzoyl chloride, 3-nitro- | HCID 8495 | — |
| 反応物 | Sodium Hydroxide | HCID 14798 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | 5-Hydroxy-4-m-nitrobenzamido-1-naphthalenesulfonic acid sodium salt | HCID 88743053 | — |
反応手順
A 43 g portion of recrystallized 8-amino-1-naphthol-5-sulfonic acid is suspended in 80 ml of water and 180 ml of 1N sodium hydroxide is added, then 66.6 g of m-nitrobenzoyl chloride is added all at once, washing in with a small amount of ether. The mixture is shaken for 5 minutes and another 180 ml of 1N sodium hydroxide is added with shaking for 1/2 hour. The latter addition of sodium hydroxide and shaking is repeated two more times. The resulting solution is filtered and the filtrate is made acid to Congo Red with hydrochloric acid, a precipitate forms which is collected by filtration. The solid is stirred with about 500 ml of ether and is filtered. This operation is repeated. The ethereal layer is then removed by vacuum siphoning and the solid is then dissolved in about 350 ml of hot water which is allowed to cool to give the product as a green solid which is collected by filtration. The product is then washed with saturated saline solution, 50% ethyl alcohol, absolute ethyl alcohol and ether.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04131684 |
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| 出典データセット | uspto-grants-1978_12 |
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| ORD ID | ord-8ee5ce0d1e794df1b81efe9249acb144 |
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| 出典メモ | uspto-grants-1978_12 |
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