HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1835632Generated: October 26, 2026
N1-(1-Methylethyl)-1,4-benzenediamine → 2,6-Di-tert-butyl4-[(4-isopropylamino-phenylamino)-methyl]-phenol
https://huagongshe.com/reaction/1835632
Participants
| Role | Name | HCID | Charge |
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| Reactant | N1-(1-Methylethyl)-1,4-benzenediamine | HCID 85306 | — |
| Reactant | Phenol, 4-(bromomethyl)-2,6-bis(1,1-dimethylethyl)- | HCID 612973 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2,6-Di-tert-butyl4-[(4-isopropylamino-phenylamino)-methyl]-phenol | HCID 12135690 | — |
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-Isopropyl-benzene-1,4-diamine (2.40 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-2,6di-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-Isopropyl-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. The product was purified using silica gel column chromatography. Product was identified by 1H-NMR. The yield of 2,6di-tert-butyl4-[(4isopropylamino-phenylamino)methyl]-phenol is 2.025 g (68%).
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-19df64c4f2e847bf9d644f7c8d2acb77 |
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| Source note | uspto-grants-2004_08 |
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