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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1176012Generated: October 26, 2026

1-[1-(Isopropylthio)ethyl]-2-nitrobenzene → 2-[1-(Isopropylthio)ethyl]aniline

https://huagongshe.com/reaction/1176012

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-[1-(Isopropylthio)ethyl]-2-nitrobenzeneHCID 57498015—
ReactantHCID 178418361HCID 178418361—
CatalystNickelHCID 935—
SolventEthanolHCID 702—
Product2-[1-(Isopropylthio)ethyl]anilineHCID 5749801687.1%

Reaction Steps

44 g (0.188 mol) 1-[1-(isopropylthio)ethyl]-2-nitrobenzene (VII-1) are dissolved in 250 ml ethanol, mixed with 3 g Raney nickel and hydrogenated in the autoclave for 6 hours at room temperature with 3 bar of hydrogen. After 6 hours another 3 g Raney nickel are added and hydrogenation is continued for another 16 hours at room temperature with 3 bar hydrogen. The catalyst is then removed by filtration and the solvent removed under vacuum. The crude product is purified by column chromatography (silica gel, 3:1 hexane/methyl t-butyl ether). 32 g (97.3% purity by HPLC, 84.4% theoretical yield) of 2-[1-(isopropylthio)ethyl]aniline are obtained as a yellow oil [logP (pH 2.3)=2.45].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07842710B2
Source datasetuspto-grants-2010_11
ORD IDord-0095de273bdc466eb92f63e88a043a39
Source noteuspto-grants-2010_11