HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1768293Generated: October 30, 2026
Phenol → 4-(3-(N-methylsulfamoyl)phenyloxy)benzene
https://huagongshe.com/reaction/1768293
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phenol | HCID 996 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-bromo-N-methylbenzene-1-sulfonamide | HCID 7213265 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-(3-(N-methylsulfamoyl)phenyloxy)benzene | HCID 23614573 | 11.4% |
Reaction Steps
To a slurry of phenol (1.9 g, 20 mmol), K2CO3 (6.0 g, 40 mmol), and CuI (4 g, 20 mmol) in DMF (25 mL) was added N-methyl-3-bromobenzenesulfonamide (2.5 g, 10 mmol), and the resulting mixture was stirred at the reflux temp. overnight, cooled to room temp., and separated between EtOAc (50 mL) and a 1 N HCl solution (50 mL). The aqueous layer was back-extracted with EtOAc (2×50 mL). The combined organic phases were sequentially washed with water (2×50 mL) and a saturated NaCl solution (50 mL), dried (MgSO4), and concentrated under reduced pressure. The residual oil was purified by column chromatography (30% EtOAc/70% hexane) to give 4-(3-(N-methylsulfamoyl)phenyloxy)benzene (0.30 g). Step 3. Synthesis of 4-(3-(N-methylsulfamoyl)phenyloxy)-1-nitrobenzene
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07235576B1 |
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| Source dataset | uspto-grants-2007_06 |
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| ORD ID | ord-368bc9d3b0d6455cbc067998e95484c8 |
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| Source note | uspto-grants-2007_06 |
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