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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1966284Generated: November 1, 2026

Methyl iodide → Methyl 3-Amino-4-chlorobenzoate

https://huagongshe.com/reaction/1966284

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantEthyl AcetateHCID 8857—
ReactantCarbonate IonHCID 19660—
Reactant3-Amino-4-chlorobenzoic acidHCID 76092—
SolventDiethyl EtherHCID 3283—
SolventDimethylformamideHCID 6228—
ProductMethyl 3-Amino-4-chlorobenzoateHCID 59305597%

Reaction Steps

3-Amino-4-chlorobenzoic acid (20.9 g, 0.122 mol) and cecium carbonate (79.5 g, 0.244 mol) were suspended in N,N-dimethylformamide (500 mL), and methyl iodide (7.60 mL, 0.122 mol) was added thereto, and then the reaction mixture was stirred under argon atmosphere at room temperature for 2 hours. Ethyl acetate (250 mL) and diethyl ether (500 mL) were added to the reaction mixture and then the whole was washed with water (1 L). The aqueous layer was extracted with ethyl acetate/diethylether (2/1) (300 mL, 3 times). The combined organic layer was washed with water (500 mL, 4 times) and saturated brine (300 mL) successively. The organic layer was dried over anhydrous magnesium sulfate and then the solvent was removed under reduced pressure to give the titled reference compound (21.82 g) as a pale brown solid. (Yield 97%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08420635B2
Source datasetuspto-grants-2013_04
ORD IDord-0653f679aebe4b1a9230f84456a855df
Source noteuspto-grants-2013_04