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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1720620Generated: October 25, 2026

Methyl iodide → N-[4-methoxybenzenesulfonyl]-(D)-asparagine methyl ester

https://huagongshe.com/reaction/1720620

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantCesium carbonateHCID 10796—
ReactantN-[4-methoxybenzenesulfonyl]-(D)-asparagineHCID 27014145—
SolventDimethylformamideHCID 6228—
SolventAmmonium ChlorideHCID 25517—
ProductN-[4-methoxybenzenesulfonyl]-(D)-asparagine methyl esterHCID 70060643—

Reaction Steps

N-[4-methoxybenzenesulfonyl]-(D)-asparagine (10.1 g, 33.3 mmol) is dissolved in dimethylformamide (167.0 mL). Cesium carbonate (5.43 g, 16.66 mmol) is added, followed by the addition of methyl iodide (2.22 mL, 33.3 mmol), and the reaction is stirred overnight. The reaction is then diluted with saturated ammonium chloride (366.0 mL), and extracted well with ethyl acetate. The combined organic extracts are washed with brine, dried (Na2SO4), and the solvent is evaporated. The crude product is recrystallized from toluene to provide N-[4-methoxybenzenesulfonyl]-(D)-asparagine methyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05506242
Source datasetuspto-grants-1996_04
ORD IDord-0c5770db3f314350967c7acc588dac9d
Source noteuspto-grants-1996_04