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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1839940Generated: October 31, 2026

Sodium Carbonate → 4-[6-(4-Fluorophenyl)-1,3-benzodioxol-5-yl]benzenesulfonamide

https://huagongshe.com/reaction/1839940

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant4-BromobenzenesulfonamideHCID 69696—
Reactant[6-(4-Fluorophenyl)-1,3-benzodioxol-5-yl]boronic acidHCID 23451199—
CatalystHCID 178418397HCID 178418397—
SolventEthanolHCID 702—
SolventTolueneHCID 1140—
Product4-[6-(4-Fluorophenyl)-1,3-benzodioxol-5-yl]benzenesulfonamideHCID 2345111376%

Reaction Steps

Under nitrogen, 500 mg of Pd(PPh3)4 was added to a stirred solution of 1.55 g (6.0 mmol) of [6-(4-fluorophenyl)-1,3-benzodioxol-5-yl]boronic acid (Step 2) and 1.09 g (4.62 mmol) of 4-bromobenzenesulfonamide (Lancaster) in 30 mL of toluene, 20 mL of ethanol, and 15 mL of 2M Na2CO3. After vigorous stirring at reflux for 6 hours, the solvent was removed in vacuo and the residue dissolved in ethyl acetate. The resulting solution was washed with water and dried over Na2SO4. Purification by silica gel chromatography (MPLC) with ethyl acetate/hexane (3:7) gave 1.3 g (76%) of 4-[6-(4-fluorophenyl)-1,3-benzodioxol-5-yl]benzenesulfonamide as a colorless solid: mp 191.0-192.5° C.; NMR (CDCl3) δ 4.80 (s, 2H), 6.06 (s, 2H), 6.83-6.92 (m, 4H), 6.97-7.06 (m, 2H), 7.20 (d, J=8.5 Hz, 2H), 7.74 (d, J=8.5 Hz, 2H). MS (FAB): m/e 372 (M+H). Anal. Calc'd for C19H14FNO4S: C, 61.45; H, 3.80; N, 3.77. Found: C, 61.48; H, 3.92; N, 3.68.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06677488B2
Source datasetuspto-grants-2004_01
ORD IDord-9caac3372dda4830a711693321f039d0
Source noteuspto-grants-2004_01