反应 #4139319
相关文献 (1)
openreactiondata ↗doi:10.1039/C8SC04228D
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-ace0925ae917468a8ae69e2ff266a308暂无可渲染的结构数据
CC(=O)N(CC(=O)O)CC(=O)O中间体产品
2-[acetyl(carboxymethyl)amino]acetic acid
结构、标识符和计算性质已按 CAS 与数据库记录完成匹配。
| 中文名称 | 2-[acetyl(carboxymethyl)amino]acetic acid |
|---|---|
| English name | 2-[acetyl(carboxymethyl)amino]acetic acid |
| IUPAC 名称 | — |
| CAS号 | 86607-56-9 |
| 数据库编号 | 10130190 |
| 分子式 | — |
| 分子量 | — |
产品信息
2-[acetyl(carboxymethyl)amino]acetic acid(CAS 86607-56-9)的产品身份、结构标识及相关反应资料,供化学中间体检索、研发和采购评估使用。
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仅供专业研发与工业用途
数据库编号 10130190
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合成路线数据
12 条反应 · 12 篇文献
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-ace0925ae917468a8ae69e2ff266a308反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-546d496cd99d4402a680168920617a8b反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-8da23f5ce95f41a7a34e9caed77cbfc0反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-2adb3da73a6b4b759eb77b5b35db564c反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-ace0925ae917468a8ae69e2ff266a308反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-ace0925ae917468a8ae69e2ff266a308反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A crude reaction mixture of N-acetyliminodiacetic acid was prepared from acetamide (5.90 g; 0.10 mol)) by the process described in French Pat. No. 2,523,576. This crude product was dissolved in a 20% aqueous hydrochloric acid solution and the resulting mixture was added to a 250 ml 3-necked flask equipped with an addition funnel and thermometer. Phosphorous acid (8.61 g; 0.105 mol) was added and the solution was heated to a temperature of 106° C.-107° C. When this temperature had been reached, formaldehyde (8.23 g of a 44% aqueous solution; 0.212 mole) was added to the mixture in the flask over a period of 30 minutes. After addition of formaldehyde was complete, the temperature was maintained at 106°-107° C. for an additional period of 3.5 hour. The reaction mixture was concentrated under reduced pressure and a precipitate formed. The product was collected by filtration to yield 14.4 g of N-phosphonomethyliminodiacetic acid (63% yield based on the starting amount of acetamide). the resulting mixture was added to a 250 ml 3-necked flask equipped with an addition funnel the solution was heated to a temperature of 106° C.-107° C 0.212 mole) was added to the mixture in the flask over a period of 30 minutes the temperature was maintained at 106°-107° C. for an additional period of 3.5 hour The reaction mixture was concentrated under reduced pressure a precipitate formed The product was collected by filtration
来源 ID: ord-c5e76f8a1a994444a628cec14edc4fd5反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A crude reaction mixture of N-acetyliminodiacetic acid was prepared from acetamide (5.90 g; 0.10 mol)) by the process described in French Pat. No. 2,523,576. This crude product was dissolved in a 20% aqueous hydrochloric acid solution and the resulting mixture was added to a 250 ml 3-necked flask equipped with an addition funnel and thermometer. Phosphorous acid (8.61 g; 0.105 mol) was added and the solution was heated to a temperature of 106° C.-107° C. When this temperature had been reached, formaldehyde (8.23 g of a 44% aqueous solution; 0.212 mole) was added to the mixture in the flask over a period of 30 minutes. After addition of formaldehyde was complete, the temperature was maintained at 106°-107° C. for an additional period of 3.5 hour. The reaction mixture was concentrated under reduced pressure and a precipitate formed. The product was collected by filtration to yield 14.4 g of N-phosphonomethyliminodiacetic acid (63% yield based on the starting amount of acetamide). the resulting mixture was added to a 250 ml 3-necked flask equipped with an addition funnel the solution was heated to a temperature of 106° C.-107° C 0.212 mole) was added to the mixture in the flask over a period of 30 minutes the temperature was maintained at 106°-107° C. for an additional period of 3.5 hour The reaction mixture was concentrated under reduced pressure a precipitate formed The product was collected by filtration
来源 ID: ord-c5e76f8a1a994444a628cec14edc4fd5反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-546d496cd99d4402a680168920617a8b反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-8da23f5ce95f41a7a34e9caed77cbfc0反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-2adb3da73a6b4b759eb77b5b35db564c反应条件: temp:195.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: N-acetyliminodiacetic acid (XVI) monohydrate (45 g) and varying amounts of water and acetic acid were heated at 175° C. or 195° C. for various periods of time. After cooling to room temperature, the mixture was filtered. The solid was washed with water (10 mL) and dried to give 1,4-di(carboxymethyl)-2,5-diketopiperazine. The table below shows the yields of solid under various conditions. After cooling to room temperature the mixture was filtered The solid was washed with water (10 mL) dried
来源 ID: ord-78a2443223b04580a874ab188fe76223PubChem References
以下资料来自该化合物的公开数据库参考记录。
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