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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 405672Generated: October 29, 2026

Water → 3-Amino-4-isopropoxy-benzenesulfonamide

https://huagongshe.com/reaction/405672

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium borohydrideHCID 4311764—
Reactant4-Isopropoxy-3-nitro-benzenesulfonamideHCID 69669064—
CatalystDichloronickel;hexahydrateHCID 11791229—
SolventMethanolHCID 887—
Product3-Amino-4-isopropoxy-benzenesulfonamideHCID 69669107—

Reaction Conditions

Temperature23 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08753857B2
Source datasetuspto-grants-2014_06
ORD IDord-0ae4d1ffe7d646adb62d32b1a55ac5e5
Source noteuspto-grants-2014_06