関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | Acetic Anhydride | HCID 7918 | — |
| 反応物 | Nitrilotriacetic Acid | HCID 8758 | — |
| 反応物 | 3-Iodo-p-toluidine | HCID 118889 | — |
| 溶媒 | Pyridine | HCID 1049 | — |
| 生成物 | 2,2'-[[2-[(3-Iodo-4-methylphenyl)amino]-2-oxoethyl]-imino]bisacetic acid | HCID 13245248 | 56.4% |
反応手順
A slurry of 4.78 g of nitrilotriacetic acid in 40 ml of dry pyridine (dried over molecular sieves) is heated to 60° C. Acetic anhydride (2.55 g) is added slowly and the solution is heated to 100° C. After heating for 0.5 hour, the solution is cooled to 40° C. and a solution of 5.8 g of 3-iodo-4-methylaniline in 20 ml of dry pyridine is added over 25 minutes. The solution is heated at 100° C. for 1.0 hour. The reaction is cooled and rotary evaporated to a residue which is dissolved in 65 ml of 10% sodium hydroxide. This solution is extracted twice with 50 ml portions of methylene chloride diluted with 100 ml of distilled water, and neutralized with concentrated HCl to pH 3.2. The crude product is refrigerated for about 16 hours, filtered, washed twice with 50 ml portions of distilled water, and dried under vacuum at 40° C. The crude product (8.0 g) is recrystallized after Darco treatment to yield 5.7 g of product, melting point 213.5°-215.0° C. (dec).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04418208 |
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| 出典データセット | uspto-grants-1983_11 |
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| ORD ID | ord-62d6e1441a1249ac9a5107a72e8e43ae |
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| 出典メモ | uspto-grants-1983_11 |
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