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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantThionyl ChlorideHCID 24386—
Reactant3-Amino-5-(aminocarbonyl)-2,4,6-triiodobenzoic acidHCID 22389716—
CatalystTetramethylureaHCID 12437—
SolventWaterHCID 962—
Product3-Amino-5-(aminocarbonyl)-2,4,6-triiodobenzoyl chlorideHCID 2146668379.8%

Reaction Conditions

Temperature74 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08680334B2
Source datasetuspto-grants-2014_03
ORD IDord-b5d1d666df324e42b2324cbaca27a1fb
Source noteuspto-grants-2014_03