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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1840859Generated: October 26, 2026

Hydrochloric Acid → 2-[3-(2,6-Dichlorophenyl)ureido]-5-iodobenzoic acid

https://huagongshe.com/reaction/1840859

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantBenzoic acid, 2-amino-5-iodo-HCID 72911—
ReactantSodium BicarbonateHCID 516892—
Reactant1,3-Dichloro-2-isocyanatobenzeneHCID 604537—
Solvent1,4-Dioxane--water (1/1)HCID 21886435—
Product2-[3-(2,6-Dichlorophenyl)ureido]-5-iodobenzoic acidHCID 2344458759.3%

Reaction Steps

To an ice cooled solution of 2-amino-5-iodobenzoic acid (540 mg, 2.03 mmol) and sodium bicarbonate (170 mg, 2.03 mmol) in 9 mL of dioxane/water (2:1) was added 2,6-dichlorophenylisocyanate (468 mg, 2.44 mmol). The reaction was slowly warmed to room temperature while stirring overnight. The reaction mixture was acidified with 2N HCl and extracted with EtOAc. The product, which partially precipitated from the organic layer, was filtered and washed with EtOAc (173 mg). The filtrate was dried (MgSO4) and evaporated under reduced pressure. Trituration of the residue with Et2O afforded an additional 543 mg of 2-[3-(2,6-dichlorophenyl)ureido]-5-iodobenzoic acid: 1H-NMR (300 MHz, d6-DMSO) δ 7.37 (t, J=8 Hz, 1H), 7.58 (d, J=8 Hz, 2H), 7.84 (dd, J=8 Hz, 4 Hz, 1H), 8.19 (d, J=4 Hz, 1H), 8.28 (d, J=8 Hz, 1H), 9.60 (s, 1H, exchangeable), 10.50 (s, 1H, exchangeable).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06683077B2
Source datasetuspto-grants-2004_01
ORD IDord-4cb5b46983124f458228010f6724820f
Source noteuspto-grants-2004_01