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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2251960Generated: November 1, 2026

Hydrochloric Acid → (2-Chlorophenyl)(2-iodophenyl)methanone

https://huagongshe.com/reaction/2251960

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantIodineHCID 807—
Reactant2-Amino-2'-chlorobenzophenoneHCID 76165—
ReactantSodium NitriteHCID 23668193—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Product(2-Chlorophenyl)(2-iodophenyl)methanoneHCID 12948264116.3%

Reaction Conditions

Temperature10 °C

Reaction Steps

Add concentrated HCl (0.5 mL) to a solution of (2-amino-phenyl)-(2-chloro-phenyl)-methanone (495 mg, 2.14 mmol) in glacial AcOH (1.1 mL). Cool solution to 10° C.; add a solution of sodium nitrite (156 mg, 2.26 mmol) in water (1 mL) dropwise over 30 min. After an additional 30 min., add water (4° C., 2 mL) and EtOAc (4° C., 4 mL). Add a solution of KI (425 mg, 2.56 mmol) and I2 (319 mg, 1.25 mmol) in water (2 mL) dropwise over 25 min. Stir at 5-15° C. for 2.5 hours under N2. Extract with EtOAc (×3), wash with 1N aqueous Na2S2O3 solution (×3), saturated aqueous NaHCO3 solution (×3) and brine. Dry the combined organic layers over Na2SO4 and concentrate. Purify the residue by flash chromatography on silica gel eluting with 0-10% EtOAc/hexanes to afford the title compound (498 mg, 68%): MS(IS) 343 (M+1); TLC (10% EtOAc/hexanes) Rf=0.39.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07320994B2
Source datasetuspto-grants-2008_01
ORD IDord-0f00eee181f84f59aaeb411c9586b43e
Source noteuspto-grants-2008_01