HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1873938Generated: November 3, 2026
Dimethyl Sulfoxide → HCID 58058451, compound
https://huagongshe.com/reaction/1873938
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | p-Fluoronitrobenzene | HCID 9590 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4,4'-Bis(1,1,3,3-tetramethylbutyl)diphenylamine | HCID 85069 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 58058451 | HCID 58058451 | 60% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08304514B2 |
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| Source dataset | uspto-grants-2012_11 |
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| ORD ID | ord-6d3b6b8bfcfc45d787fdb7bfdb16d369 |
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| Source note | uspto-grants-2012_11 |
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