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HRID 65903作成日:2026年10月25日
5-Nitroisophthaloyl chloride → 3,3'-[(5-Nitro-1,3-phenylene)bis(carbonylimino)]bis[2,7-naphthalenedisulfonic acid] tetrasodium salt
https://huagongshe.com/reaction/65903
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 5-Nitroisophthaloyl chloride | HCID 83451 | — |
| 反応物 | Sodium Acetate | HCID 517045 | — |
| 反応物 | Sodium 3-amino-7-sulfonaphthalene-2-sulfonate | HCID 23702076 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | 3,3'-[(5-Nitro-1,3-phenylene)bis(carbonylimino)]bis[2,7-naphthalenedisulfonic acid] tetrasodium salt | HCID 131711362 | — |
反応手順
A 6.5 g portion of 3-amino-2,7-naphthalenedisulfonic acid monosodium salt is suspended in 100 ml of water and the pH is adjusted to 7.5-8.0 giving a solution. A 1.82 g portion of sodium acetate is added and dissolved and 2.75 g of 5-nitro-1,3-benzenedicarbonylchloride is added. A 100 ml portion of water is added to maintain solution and the reaction is allowed to stand overnight. The mixture is treated with activated carbon and concentrated to about 50 ml on a rotary evaporator. The solid which forms is redissolved by heating on a steam bath. Cooling produces crystals which are dried overnight in an Abderhalden under high vacuum and refluxing toluene to give 3,3'-[(5-nitro-1,3-phenylene)bis(carbonylimino)]bis[2,7-naphthalenedisulfonic acid] tetrasodium salt.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04129591 |
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| 出典データセット | uspto-grants-1978_12 |
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| ORD ID | ord-ddaf2aeebe944b5282aa00472c27ec11 |
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| 出典メモ | uspto-grants-1978_12 |
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