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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1662730Generated: October 26, 2026

1,2,3-Trimethoxybenzene → 2,3,4-trimethoxybenzenesulfonyl Chloride

https://huagongshe.com/reaction/1662730

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2,3-TrimethoxybenzeneHCID 12462—
ReactantChlorosulfonic acidHCID 24638—
ReactantPhosphorus oxychlorideHCID 24813—
SolventChloroformHCID 6212—
Product2,3,4-trimethoxybenzenesulfonyl ChlorideHCID 47127422.8%

Reaction Steps

To a solution of 10.0 g of 1,2,3-trimethoxy benzene in CHCl3 (100 ml) was added dropwise 6.90 g of chlorosulfonic acid over 10 minutes under ice cooling. After stirring at room temperature for two hours, the solution was poured into ice water and the resulting mixture was extracted with CHCl3. The aqueous layer was filtered with celite, the filtrate was neutralized with an aqueous solution of 2 mol/L KOH (pH=9), and the solvent was evaporated under reduced pressure to obtain 1.40 g. Phosphorus oxychloride (7 ml) was added to the obtained residue and the mixture was stirred at external temperature of 100° C. for one hour. The solution was poured into ice water, the resulting mixture was extracted with Et2O, the organic layer was washed with water and with saturated brine and then dried over MgSO4; the drying agent was separated by filtration, and then the solvent was evaporated under reduced pressure. The obtained residue was purified by column chromatography (silicagel 60N; mobile phase: EtOAc/n-hexane=1/10 to 1/4; v/v) to obtain 450 mg of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08030499B2
Source datasetuspto-grants-2011_10
ORD IDord-bd3213e4ef694c818a724d3c69f32467
Source noteuspto-grants-2011_10