Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1835630Generated: November 3, 2026

Phenol, 4-(bromomethyl)-2,6-bis(1,1-dimethylethyl)- → HCID 12135691, compound

https://huagongshe.com/reaction/1835630

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenol, 4-(bromomethyl)-2,6-bis(1,1-dimethylethyl)-HCID 612973—
Reactant1,4-Benzenediamine, N1-(1,4-dimethylpentyl)-HCID 6454574—
SolventTetrahydrofuranHCID 8028—
ProductHCID 12135691HCID 12135691—

Reaction Steps

4Bromomethyl-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(1,4-Dimethyl-pentyl)-benzene-1,4-diamine (3.28 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-bottom flask containing solution of 4-Bromomethyl-2,6-di-tert-butyl-phenol was kept in oil-bath at temperature 85° C. Solution in the flask was continuously stirred with the help of magnetic stirrer. N(1,4-Dimethyl-pentyl)-benzene-1,4diamine 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-(1,4-dimethyl-pentylamino)-phenylamino)methyl}-phenol is 2. 29 g (67%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06770785B1
Source datasetuspto-grants-2004_08
ORD IDord-fac1c6fd5caa4ea9b9af604451774d41
Source noteuspto-grants-2004_08