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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1968446Generated: October 29, 2026

Iodine → Benzoic acid, 4-amino-2-chloro-5-iodo-, methyl ester

https://huagongshe.com/reaction/1968446

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantDichloromethaneHCID 6344—
ReactantCalcium CarbonateHCID 10112—
ReactantBenzoic acid, 4-amino-2-chloro-5-iodo-, methyl esterHCID 11839203—
SolventMethanolHCID 887—
ProductBenzoic acid, 4-amino-2-chloro-5-iodo-, methyl esterHCID 11839203—
ProductMethyl 4-amino-2-chloro-3-iodobenzoateHCID 59625863—

Reaction Steps

Methyl 4-amino-2-chloro-5-iodo-benzoate, 70n. To a suspension of compound 70m (1.18 g, 6.38 mmol) and CaCO3 (12.8 mmol, 1.28 g) in MeOH (13 mL) was added a solution of iodine monchloride (6.70 mmol, 1.09 g) in CH2Cl2 (6 mL) dropwise at room temperature. The resulting reaction mixture was stirred at room temperature for 1.5 h. The reaction mixture was concentrated and then partitioned between EtOAc and water. The organic layer was concentrated and purified by flash column chromatography (silica gel, 20-25% EtOAc/hexanes) to provide methyl 4-amino-2-chloro-5-iodo-benzoate 70n as major the product and methyl 4-amino-2-chloro-3-iodo-benzoate 70o as the minor product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08426401B2
Source datasetuspto-grants-2013_04
ORD IDord-60af97b291694a1a8d8de4a4e3a5b00a
Source noteuspto-grants-2013_04