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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1873938Generated: November 3, 2026

Dimethyl Sulfoxide → HCID 58058451, compound

https://huagongshe.com/reaction/1873938

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
Reactantp-FluoronitrobenzeneHCID 9590—
ReactantSodium hydrideHCID 24758—
Reactant4,4'-Bis(1,1,3,3-tetramethylbutyl)diphenylamineHCID 85069—
SolventMethanolHCID 887—
ProductHCID 58058451HCID 5805845160%

Reaction Conditions

Temperature120 °C

Reaction Steps

First, 76.20 mmol of Bis-(4-(2,4,4-trimethylpentan-2-yl)phenyl)amine, 91.45 mmol of 4-Fluoronitrobenzene, 114.31 mmol of sodium hydride, 2.74 g of NaH, and 120 ml of dimethyl sulfoxide (DMSO) were added into a bottle. After stirring at 120° C. for 48 hrs, the reaction mixture was cooled and then poured into 1 L of methanol. The yellow precipitate was collected by filtration and dried under vacuum. The product was purified by silica gel column chromatography (dichloromethane:n-hexane=1:3) and recrystallized from ethyl acetate to afford 4-nitro-N,N-bis(4-(2,4,4-trimethylpentan-2-yl)phenyl)aniline as a yellow crystal with a yield of 60%. The 4-nitro-N,N-bis(4-(2,4,4-trimethylpentan-2-yl)phenyl)aniline had a melt point of 167° C. The synthesis pathway was as follows:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08304514B2
Source datasetuspto-grants-2012_11
ORD IDord-6d3b6b8bfcfc45d787fdb7bfdb16d369
Source noteuspto-grants-2012_11