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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1603006Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/1603006

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktBenzoic acid, 2-amino-5-iodo-HCID 72911—
EduktSodium BicarbonateHCID 516892—
Edukt1,3-Dichloro-2-isocyanatobenzeneHCID 604537—
Lösungsmittel1,4-Dioxane--water (1/1)HCID 21886435—
Produkt2-[3-(2,6-Dichlorophenyl)ureido]-5-iodobenzoic acidHCID 2344458759,3%

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05985872
Quelldatensatzuspto-grants-1999_11
ORD IDord-fd94c897d4b94e37bbf90c7b3f105a4d
Quellennotizuspto-grants-1999_11