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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1293465Generated: October 30, 2026

Hydrochloric Acid → 4-Methoxy-dibenzo[b,d]furan-1-sulfonyl chloride

https://huagongshe.com/reaction/1293465

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSulfur DioxideHCID 1119—
Reactant4-Methoxydibenzofuran-1-amineHCID 459356—
ReactantSodium NitriteHCID 23668193—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
SolventAcOH benzeneHCID 22229412—
Product4-Methoxy-dibenzo[b,d]furan-1-sulfonyl chlorideHCID 85967102—

Reaction Conditions

Temperature5 °C

Reaction Steps

Intermediate 40 (400 mg, 1.87 mmol) was dissolved in glacial acetic acid (20 ml) and 17% HCl (10 ml). This solution was cooled to 5° C. and a solution of sodium nitrite (260 mg, 3.74 mmol) in water (5 ml) was added slowly during 10 min. The reaction was stirred for 1 h at 5° C. The reaction mixture was then added to a saturated solution of sulfur dioxide (generated from sodium sulfite and conc. HCl) in acetic acid: benzene (3:2) containing cupric chloride dihydrate (100 mg, 0.513 mmol). The reaction was sired at room temperature for 20 h and then poured water (500 ml) and extracted with ethyl acetate (3×100 ml). The extract was washed with water (5×100 ml) and dried over anhydrous sodium sulfate. The solvent was evaporated to give the product as brown solid (350 mg) which was directly used to make the sulfonamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07238725B2
Source datasetuspto-grants-2007_07
ORD IDord-70bd2ef2d4e04aebb7c3cfe323b26941
Source noteuspto-grants-2007_07