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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2255650Generated: November 1, 2026

Pyridine → HCID 19737610, compound

https://huagongshe.com/reaction/2255650

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantAcetic AnhydrideHCID 7918—
Reactant4-IodoanilineHCID 10893—
Reactant5-Iodo-2-benzofuran-1,3-dioneHCID 15263377—
SolventWaterHCID 962—
SolventDimethylacetamideHCID 31374—
ProductHCID 19737610HCID 19737610—

Reaction Conditions

Temperature70 °C

Reaction Steps

##STR19## A 100 milliliter round-bottomed flask, equipped with stirrer, was charged with p-iodoaniline (10.95 grams, 0.05 mol) and dimethylacetamide (DMAc) (35 milliliters). 4-iodophthalic anhydride (13.6 grams, 0.05 mol) was added slowly over 10 minutes. The reaction mixture was heated with stirring to a temperature of about 70° C. Pyridine (19.45 grams, 0.25 mol) was added, the reaction mixture was stirred for 15 minutes, then acetic anhydride (11.12 grams, 0.11 mol) was added dropwise over 20 minutes. The reaction mixture was stirred at 70° C. overnight. The reaction mixture was poured into water, producing a white solid product, which was collected by filtration, triturated with methanol (300 milliliters) and dried under vacuum at 60° C. overnight. Melting point, as determined by DSC was 235° C. Combustion analysis was: calculated: C=35.40, H=1.49, N=2.95; measured: C=35.47, H=1.59, N=2.94. Proton NMR was consistent with the above general structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05241038
Source datasetuspto-grants-1993_08
ORD IDord-9ff793e2ac0b4ffcb65128a1e6821e0d
Source noteuspto-grants-1993_08