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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2071118Generated: November 2, 2026

Methyl iodide → Dimethyl 5-(N-methylmethylsulfonamido)isophthalate

https://huagongshe.com/reaction/2071118

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantDimethyl 5-(methylsulfonamido)isophthalateHCID 3711983—
SolventDimethylformamideHCID 6228—
ProductDimethyl 5-(N-methylmethylsulfonamido)isophthalateHCID 11324067—

Reaction Steps

To a stirred suspension of NaH (0.24 g, 10 mmol, 60% in oil dispersion) in 10 mL of DMF was added dimethyl 5-(methylsulfonamido)isophthalate (1.435 g, 5 mmol) followed by iodomethane (0.62 mL, 10 mmol) at room temperature. After 5 h, the reaction was quenched by H2O (25 mL). Then the reaction mixture was extracted with EtOAc, further washed with H2O to remove excess of DMF, dried over anhydrous Na2SO4 and concentrated. The crude product thus obtained was washed with hexanes to give dimethyl 5-(N-methylmethylsulfonamido)isophthalate as a white solid in 91% (1.37 g) yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08299267B2
Source datasetuspto-grants-2012_10
ORD IDord-8d7e507390404a2e8d7badc1f9135198
Source noteuspto-grants-2012_10