HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 333585Generated: October 29, 2026
Water → 3-Amino-4-isopropoxy-benzenesulfonamide
https://huagongshe.com/reaction/333585
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 4-Isopropoxy-3-nitro-benzenesulfonamide | HCID 69669064 | — |
| Catalyst | Dichloronickel;hexahydrate | HCID 11791229 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 3-Amino-4-isopropoxy-benzenesulfonamide | HCID 69669107 | — |
Reaction Steps
Sodium borohydride (1.88 g, 49.6 mmol) was added slowly to a solution of nickel (II) chloride hexahydrate (3.93 g, 16.5 mmol) in methanol (60 mL) at 0° C. and the resulting black suspension was stirred for 30 min at 23° C. The mixture was cooled to 0° C. and 4-isopropoxy-3-nitro-benzenesulfonamide (8.6 g, 33.0 mmol, example 2, step c) was added followed by sodium borohydride (4.38 g, 115.6 mmol). The resulting black suspension was stirred for 30 min at 23° C. Water was added to the reaction mixture to quench excess NaBH4, followed by addition of saturated aqueous NaHCO3. The product was extracted with dichloromethane and the organic phase was washed with brine, dried with Na2SO4 and evaporated to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08883473B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-0208af1266e342db8483b4ef773e0e50 |
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| Source note | uspto-grants-2014_11 |
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