HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2184895Generated: October 27, 2026
Water → N-tert-butyl-4'-aminobiphenyl-2-sulfonamide
https://huagongshe.com/reaction/2184895
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 4-Bromoaniline | HCID 7807 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Boronic acid, B-(2-(((1,1-dimethylethyl)amino)sulfonyl)phenyl)- | HCID 4997616 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | N-tert-butyl-4'-aminobiphenyl-2-sulfonamide | HCID 10804475 | — |
Reaction Steps
To a solution of 2-[(tert-butyl amino)sulfonyl]phenyl boronic acid (6.00 g, 23.35 mmol) in 120 ml toluene was added water (16 ml), isopropanol (60 ml), and NaOH (40 ml, 5M aqueous solution). To this were added 4-bromoaniline and Pd(Ph3P)4. This heterogeneous mixture is then refluxed for 6 hr, then stirred at room temperature over night before refluxing for another 1.5 hr. The reaction mixture is then extracted with water and ethyl acetate. The aqueous layer is extracted twice with ethyl acetate. The organic layers are then dried over MgSO4, filtered and concentrated in vacuo. The crude residue is purified by silica gel flash chromatography. The desired product can be eluded with 30% ethyl acetate in hexanes and concentrated to an orange solid (5.06 g, 16.65, 71%). ES-MS(M+H)+=305.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06399627B1 |
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| Source dataset | uspto-grants-2002_06 |
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| ORD ID | ord-e740469c14e74eaa850bdbd818657eae |
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| Source note | uspto-grants-2002_06 |
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