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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2390156Generated: October 30, 2026

4-(methylsulfonyl)-2-nitro-1-[(1E)-prop-1-en-1-yl]benzene → 5-(methylsulfonyl)-2-[(1E)-prop-1-en-1-yl]aniline

https://huagongshe.com/reaction/2390156

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(methylsulfonyl)-2-nitro-1-[(1E)-prop-1-en-1-yl]benzeneHCID 58521984—
CatalystIronHCID 23925—
SolventAcetic AcidHCID 176—
Product5-(methylsulfonyl)-2-[(1E)-prop-1-en-1-yl]anilineHCID 5852201381.4%

Reaction Conditions

Temperature90 °C

Reaction Steps

A solution of 4-(methylsulfonyl)-2-nitro-1-[(1E)-prop-1-en-1-yl]benzene (Intermediate 59; 1.10 g; 4.56 mmol) in AcOH (7 ml) was treated with powdered iron (3.82 g; 68.4 mmol) and the reaction mixture was stirred at 90° C. for 25 min. Further AcOH was added (20 mL), the solid was filtered off and rinsed with EtOAc. The solvents were removed under reduced pressure, the residue was taken up in EtOAc and washed with saturated NaHCO3 solution twice the with brine. The organic phase was dried on MgSO4, filtered and concentrated under reduced pressure to give the title compound as a brown oil (784 mg, 81%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08273769B2
Source datasetuspto-grants-2012_09
ORD IDord-55328cad460c4d87b5cd0170de8399c1
Source noteuspto-grants-2012_09