HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 76839Erstellt: 24. Oktober 2026
Water → (S)-(-)-5-[(2-Acetoxypropanoyl)amino]-2,4,6-triiodoisophthalic Acid
https://huagongshe.com/de/reaction/76839
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Water | HCID 962 | — |
| Edukt | 5-Amino-2,4,6-triiodo-1,3-benzenedicarboxylic acid | HCID 3015783 | — |
| Edukt | (1S)-2-Chloro-1-methyl-2-oxoethyl acetate | HCID 11094804 | — |
| Lösungsmittel | Dimethylacetamide | HCID 31374 | — |
| Produkt | (S)-(-)-5-[(2-Acetoxypropanoyl)amino]-2,4,6-triiodoisophthalic Acid | HCID 15817302 | 57,5% |
Reaktionsschritte
(S)-1-chloro-1-oxopropan-2-yl acetate (0.75 ml, 5.91 mmol) was added drop-wise to a solution of 5-amino-2,4,6-triiodoisophthalic acid (1.0 g, 1.79 mmol) in DMA (5 ml). The resulting mixture was stirred at about 50° C. for 5 hours and 20 minutes. 80 ml of water was added to the reaction mixture at room temperature after which the suspension formed was cooled to a temperature between 0° C. and 5° C. and stirred for 25 minutes at this temperature. The suspension was filtered and the solid washed with water. The product was dried in a vacuum oven at 40° C. to yield (S)-5-(2-acetoxypropanamido)-2,4,6-triiodoisophthalic acid (0.695 g, 1.03 mmol). The MS, 1H-NMR and 13C-NMR data are consistent with the structure for (S)-5-(2-acetoxypropanamido)-2,4,6-triiodoisophthalic acid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08835672B2 |
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| Quelldatensatz | uspto-grants-2014_09 |
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| ORD ID | ord-ab0b12a16a294dd3a941a09e08b3714b |
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| Quellennotiz | uspto-grants-2014_09 |
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