HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1192993Generated: November 1, 2026
Ethyl Acetate → 3-Amino-5-(aminocarbonyl)-2,4,6-triiodobenzoyl chloride
https://huagongshe.com/reaction/1192993
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 3-Amino-5-(aminocarbonyl)-2,4,6-triiodobenzoic acid | HCID 22389716 | — |
| Catalyst | Tetramethylurea | HCID 12437 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-Amino-5-(aminocarbonyl)-2,4,6-triiodobenzoyl chloride | HCID 21466683 | 79.8% |
Reaction Steps
A 4000 L glass-lined reactor was charged with ethyl acetate (2250 kg), 3-amino-5-(aminocarbonyl)-2,4,6-triiodobenzoic acid (1125 kg) and tetramethylurea (4.75 kg). The reaction mixture was stirred and heated to 74° C. Thionyl chloride (528 kg) was charged over 1 hour. The reaction mixture was maintained at 74° C. for 12 hours. While cooling to 45° C., additional ethyl acetate (180 kg) was charged. Water (73 kg) was charged over 1 hour and the reaction mixture was cooled to 28° C. After stirring for 7 hours, the solid product was isolated by filtration and the solids were washed with ethyl acetate (250 kg). After drying at 40° C. under vacuum, 927 kg of 3-amino-5-(aminocarbonyl)-2,4,6-triiodobenzoyl chloride were isolated which had a chromatographic purity of 92.4 area %.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08680334B2 |
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| Source dataset | uspto-grants-2014_03 |
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| ORD ID | ord-b5d1d666df324e42b2324cbaca27a1fb |
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| Source note | uspto-grants-2014_03 |
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