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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2263939Generated: October 29, 2026

Diazomethane → 5-Chlorosulfonyl-2-ethoxy-4-methoxy-benzoic acid methyl ester

https://huagongshe.com/reaction/2263939

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiazomethaneHCID 9550—
ReactantHCID 86612878HCID 86612878—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Product5-Chlorosulfonyl-2-ethoxy-4-methoxy-benzoic acid methyl esterHCID 86612879—

Reaction Steps

A solution of 5-chlorosulfonyl-2-ethoxy-4-methoxybenzoic acid (13 g, 44 mmol) in tetrahydrofuran was cooled to 5° C. and treated with excess diazomethane in ether solution (prepared from N-methyl-N-nitroso-p-toluenesulfonamide, Aldrich) and stirred for 10 min. Solvent and excess diazomethane was removed by rotary evaporation. The resulting residue was dissolved in dichloromethane and filtered through a plug of silica gel and evaporated. The solids were triturated with ether/hexane to give 13 g of 5-chlorosulfonyl-2-ethoxy-4-methoxy-benzoic acid methyl ester as a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07851626B2
Source datasetuspto-grants-2010_12
ORD IDord-16d1047071434a33bc38acf8d9291a3e
Source noteuspto-grants-2010_12