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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1830076Generated: November 1, 2026

Iodine → Benzoic acid, 4-iodo-2-methoxy-, methyl ester

https://huagongshe.com/reaction/1830076

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantSulfuric AcidHCID 1118—
ReactantPotassium IodideHCID 4875—
ReactantMethyl 4-amino-o-anisateHCID 168705—
ReactantSodium NitriteHCID 23668193—
SolventWaterHCID 962—
ProductBenzoic acid, 4-iodo-2-methoxy-, methyl esterHCID 2261946855.7%

Reaction Steps

4-Amino-2-methoxybenzoic acid methyl ester (3.0 g, 16.6 mmol) was suspended in water (40 mL) and concentrated sulfuric acid (10 mL). The suspension was cooled in an ice/salt water bath, and an aqueous solution (10 mL) of sodium nitrite (1.26 g, 18.3 mmol) was added dropwise so that the temperature remained close to 0° C. After the addition, a homogeneous, yellow-green solution was obtained. An aqueous solution (60 mL) of potassium iodide (3.02 g, 18.2 mmol) and iodine (2.31 g, 9.1 mmol) was then added dropwise, and the reaction stirred for an additional 1 hour. The reaction mixture was then extracted with ethyl acetate, the organic extracts were combined and washed with 1 N sodium thiosulfate, 1 N sodium hydroxide and brine. After drying over anhydrous sodium sulfate the solution was filtered and concentrated in vacuo to give 2.7 g of the title product as an orange oil which was used in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07064120B2
Source datasetuspto-grants-2006_06
ORD IDord-c1912724b6a044a389dad0f379552a34
Source noteuspto-grants-2006_06