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HRID 76840作成日:2026年10月25日
5-Amino-2,4,6-triiodo-1,3-benzenedicarboxylic acid → (S)-(-)-5-[(2-Acetoxypropanoyl)amino]-2,4,6-triiodoisophthalic Acid
https://huagongshe.com/reaction/76840
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | 5-Amino-2,4,6-triiodo-1,3-benzenedicarboxylic acid | HCID 3015783 | — |
| 反応物 | (1S)-2-Chloro-1-methyl-2-oxoethyl acetate | HCID 11094804 | — |
| 溶媒 | Dimethylacetamide | HCID 31374 | — |
| 生成物 | (S)-(-)-5-[(2-Acetoxypropanoyl)amino]-2,4,6-triiodoisophthalic Acid | HCID 15817302 | 81% |
反応手順
(S)-1-chloro-1-oxopropan-2-yl acetate (37.4 ml, 295.4 mmol) was added slowly to a suspension of 5-amino-2,4,6-triiodoisophthalic acid (50.0 g, 89.5 mmol) in DMA (100 ml) at a temperature of between 25° C. and 29° C. The resulting mixture was heated to about 50° C. and stirred at this temperature for about 8 hours after which heating was removed and the mixture was stirred for about 14 hours at room temperature. The reaction mixture was added slowly over water (500 ml) with strong stirring at a temperature between 22° C. and 30° C. After addition 300 ml of water were added to the suspension. The suspension was stirred for 5 further hours at about 22° C. after which the white solid was filtered and washed with water previously cooled at about 5° C. twice (30 ml each time). The product was dried in a vacuum oven at about 5.0° C. to yield (S)-5-(2-acetoxypropanamido)-2,4,6-triiodoisophthalic acid (48.8 g, 72.5 mmol).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08835672B2 |
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| 出典データセット | uspto-grants-2014_09 |
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| ORD ID | ord-3de18174c3394887ab022402120c5a28 |
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| 出典メモ | uspto-grants-2014_09 |
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