Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzene | HCID 241 | — |
| Reactant | Sulfanilic acid | HCID 8479 | — |
| Reactant | Trifluoroacetic anhydride | HCID 9845 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | 4-(Phenylsulfonyl)aniline | HCID 516666 | — |
Reaction Steps
A mixture of sulfanilic acid (10 g, 0.52 mmol), benzene (4.7 g, 0.56 mmol) and trifluoroacetic anhydride (42 g) in trifluoroacetic acid (42 g) was heated to reflux for 3 days. The solvent was removed in vacuo and the residue taken up in 10% aqueous sodium hydroxide and heated to 100° C. for 15 minutes. The resulting white precipitate was filtered off, washed with water and dried to give [4-(phenylsulfonyl)phenyl]amine. 1H NMR (400 MHz, d6-DMSO) δ 7.83-7.81 (2H, m), 7.61-7.51 (5H, m), 6.62-6.58 (2H, m), 6.15 (2H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07592456B2 |
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| Source dataset | uspto-grants-2009_09 |
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| ORD ID | ord-283f2a691f9945d2a83777d64e8bb43a |
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| Source note | uspto-grants-2009_09 |
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