HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1768294Generated: October 31, 2026
4-(3-(N-methylsulfamoyl)phenyloxy)benzene → 4-(3-(N-methylsulfamoyl)phenyloxy)-1-nitrobenzene
https://huagongshe.com/reaction/1768294
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-(3-(N-methylsulfamoyl)phenyloxy)benzene | HCID 23614573 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | 4-(3-(N-methylsulfamoyl)phenyloxy)-1-nitrobenzene | HCID 23614572 | 56.9% |
Reaction Steps
To a solution of 4-(3-(N-methylsulfamoyl)phenyloxy)benzene (0.30 g, 1.14 mmol) in TFA (6 mL) at −10° C. was added NaNO2 (0.097 g, 1.14 mmol) in portions over 5 min. The resulting solution was stirred at −10° C. for 1 h, then was allowed to warm to room 5 temp., and was concentrated under reduced pressure. The residue was separated between EtOAc (10 mL) and water (10 mL). The organic phase was sequentially washed with water (10 mL) and a saturated NaCl solution (10 mL), dried (MgSO4) and concentrated under reduced pressure to give 4-(3-(N-methylsulfamoyl)phenyloxy)-1-nitrobenzene (0.20 g). This material carried on to the next step without further purification. Step 4. Synthesis of 4-(3-(N-methylsulfamoyl)phenyloxy)aniline
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-f864796e59b041dba6a408f347ea2eef |
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| Source note | uspto-grants-2007_06 |
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