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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2040433Generated: October 30, 2026

Potassium Carbonate → HCID 57517767, compound

https://huagongshe.com/reaction/2040433

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantSulfuryl chlorideHCID 24648—
Reactant2,4-Dimethoxybenzenesulfonyl chlorideHCID 2734626—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 57517766HCID 57517766—
SolventDimethylformamideHCID 6228—
ProductHCID 57517767HCID 5751776718.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

Potassium tert-butoxide (1.21 g, 10.8 mmol) was added to an ice-cold solution of the intermediate from Step A (3.00 g, 10.8 mmol) in DMF (30 ml), and the mixture was stirred at 0° C. for 30 min. After addition of 2,4-dimethoxy-benzenesulfonyl chloride (2.5 g, 10.8 mmol), the reaction mixture was left to stir at 0° C. for 1 hour. Further addition of 0.2 equivalent each of potassium tert-butoxide and sulfonyl chloride led to no further advance in the reaction according to thin-layer chromatography. The reaction mixture was stirred into dilute potassium carbonate solution, and the resulting precipitate was filtered off. The precipitate was taken up in ethyl acetate, and the extract was washed with saturated brine and dried over magnesium sulfate. Purification by chromatography (silica gel, gradient 30% to 50% ethyl acetate in heptane) and recrystallization from diethyl ether resulted in 0.96 g of the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08580842B2
Source datasetuspto-grants-2013_11
ORD IDord-0c1d586ce0774cebaa5079f904f7f5e6
Source noteuspto-grants-2013_11