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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 359455Generated: October 29, 2026

1-(Methanesulfonylmethyl)-4-nitrobenzene → 4-[(methylsulfonyl)methyl]aniline(SALTDATA: FREE)

https://huagongshe.com/reaction/359455

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(Methanesulfonylmethyl)-4-nitrobenzeneHCID 287370—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthyl AcetateHCID 8857—
Product4-[(methylsulfonyl)methyl]aniline(SALTDATA: FREE)HCID 1284396455.2%

Reaction Steps

A solution of 1-[(methylsulphonyl)methyl]-4-nitrobenzene (4 g) in ethyl acetate (300 ml) containing a catalytic amount of palladium on carbon (10%, prehydrogenated, 0.5 g) was hydrogenated at room temperature and pressure until hydrogen uptake ceased (1400 ml, 1 h). The catalyst was filtered off and the filter cake washed with warm ethanol (2×80 ml). The filtrates were combined and concentrated under vacuum to afford the title compound (1.9 g) as a pale yellow crystalline solid, m.p. 167°-168° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05001135
Source datasetuspto-grants-1991_03
ORD IDord-f8bc6ecea16644b99610ca9b3f5cb226
Source noteuspto-grants-1991_03