HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1835631Generated: November 1, 2026
N-Phenyl-p-phenylenediamine → HCID 20268565, compound
https://huagongshe.com/reaction/1835631
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-Phenyl-p-phenylenediamine | HCID 7564 | — |
| Reactant | Phenol, 4-(bromomethyl)-2,6-bis(1,1-dimethylethyl)- | HCID 612973 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 20268565 | HCID 20268565 | — |
Reaction Steps
4-Bromomethyl-2,6-di-tert-butyl-phenol (2.42 g, 0.008 mole) was dissolved in 50 mL of dry tetrahydrofuran . In a separate conical flask N-Phenyl-benzene-1,4-diamine (2.93 g, 0.016 mole) was dissolved in 25 mL of tetrahydrofuran and solution was transferred to a cylindrical funnel with pressure equalizing tube. Three-necked round-bottomed flask containing solution of 4-Bromomethyl-2,6-di-tert-butyl-phenol was kept in oil-bath at 85° C. Solution in the flask was continuously stirred with the help of magnetic stirrer. N-Phenyl-benzene-1,4-diamine solution was added drop-by-drop, from funnel to the flask in acidic medium for a span of 4-5 hours till all the solution was poured out. The reaction was terminated after that and the final reaction mixture was allowed to attain room temperature. Product was separated by solvent evaporation. The product was purified using silica gel column chromatography. Product was identified by 1H-NMR. The yield of 2,6-di-tert-butyl-4-[(4-phenylamino-phenylamino)phenol is 2.044 g (63%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06770785B1 |
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| Source dataset | uspto-grants-2004_08 |
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| ORD ID | ord-e88fefde1bd447b79bab170c8a890dec |
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| Source note | uspto-grants-2004_08 |
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