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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 4-Bromobenzenesulfonamide | HCID 69696 | — |
| Reactant | [6-(4-Fluorophenyl)-1,3-benzodioxol-5-yl]boronic acid | HCID 23451199 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 4-[6-(4-Fluorophenyl)-1,3-benzodioxol-5-yl]benzenesulfonamide | HCID 23451113 | 76% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06677488B2 |
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| Source dataset | uspto-grants-2004_01 |
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| ORD ID | ord-9caac3372dda4830a711693321f039d0 |
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| Source note | uspto-grants-2004_01 |
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