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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 588775Generated: October 30, 2026

Ethyl oxoacetate → Ethyl 2-((4-chloro-5-iodo-2-methoxyphenyl)amino)acetate

https://huagongshe.com/reaction/588775

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl oxoacetateHCID 70211—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant4-Chloro-5-iodo-2-methoxyanilineHCID 91758377—
CatalystAcetic AcidHCID 176—
SolventMethanolHCID 887—
ProductEthyl 2-((4-chloro-5-iodo-2-methoxyphenyl)amino)acetateHCID 92135552109.8%

Reaction Steps

To a solution of 4-chloro-5-iodo-2-methoxybenzenamine (6 g, 21.2 mmol) in MeOH (50 mL) at room temperature, AcOH (3 drops) and ethyl glyoxalate (5.6 g, 27.5 mmol, 50% in toluene) were added. The mixture was stirred at room temperature for 2 h and then sodium cyanoborohydride (5.32 g, 84.8 mmol) was added to the mixture. The resulting mixture was stirred at 50° C. for 16 h. The mixture was allowed to cool to room temperature, and partitioned between ethyl acetate and water. The organic layer was dried over MgSO4, filtered, and concentrated in vacuo to afford the crude product (8.6 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09227978B2
Source datasetuspto-grants-2016_01
ORD IDord-6df1f413d8344de7a3a6f817e8c34174
Source noteuspto-grants-2016_01