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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1446443Generated: November 1, 2026

Potassium Iodide → Methyl 4-[formyl-(2-oxopropyl)amino]-3-methoxybenzoate

https://huagongshe.com/reaction/1446443

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantChloroacetoneHCID 6571—
ReactantCesium carbonateHCID 10796—
ReactantMethyl 4-formamido-3-methoxybenzoateHCID 23085082—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductMethyl 4-[formyl-(2-oxopropyl)amino]-3-methoxybenzoateHCID 86602464—

Reaction Steps

Chloroacetone (84.5 mL) was added dropwise to the DMF (497 mL) mixture of 4-formylamino-3-methoxybenzoic acid methyl ester (111 g), cesium carbonate (346 g), and potassium iodide (8.78 g) at room temperature, and the reaction mixture was agitated for 3 hours. Cesium carbonate (173 g) and chloroacetone (42.0 mL) were added to the reaction mixture, and the reaction mixture was agitated at room temperature for 2 hours. Iced water and ethyl acetate were added to the reaction mixture, and the organic layer was partitioned. Ethyl acetate was added to the aqueous layer and the organic layer was partitioned. The organic layers were combined, washed with water and a saturated saline solution in this order, and the obtained organic layer was dried over anhydrous magnesium sulfate and then concentrated under reduced pressure. The residue was diluted with toluene and the solution was concentrated under reduced pressure. Tert-butylmethyl ether and heptane were added to the resulted residue and the deposited solids were separated by filtering and washed with a 50% heptane solution of tert-butylmethyl ether. 118 g of the title compound was obtained by air-drying the obtained solids overnight.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07667041B2
Source datasetuspto-grants-2010_02
ORD IDord-3164b0df79c947279236bef1371c4755
Source noteuspto-grants-2010_02