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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 502805Generated: November 2, 2026

Chloromethyl Methyl Ether → HCID 59428123, compound

https://huagongshe.com/reaction/502805

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloromethyl Methyl EtherHCID 7864—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 59428157HCID 59428157—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59428123HCID 59428123—

Reaction Steps

To a solution of N-(2-bromo-4-chloro-phenyl)-4-tert-butyl-benzenesulfonamide (1.00 g, 2.49 mmol) and K2CO3 (1.72 g, 12.4 mmol) in 8 mL anhydrous THF was added chloromethyl methyl ether (299 mg, 3.73 mmol). The resultant heterogeneous solution was stirred for 60 minutes at ambient temperature and the solids were subsequently removed via filtration. The filtrate was subsequently concentrated in vacuo and the residue was dissolved in EtOAc. The organics were washed with saturated Na2CO3, dried over MgSO4, and evaporated in vacuo. The resultant residue was then purified via automated silica gel chromatography to afford the desired protected sulfonamide: MS (ES) M+H expected 446.0, found 446.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07776877B2
Source datasetuspto-grants-2010_08
ORD IDord-305c797e9ccc40948d1daa2eb3ed5034
Source noteuspto-grants-2010_08