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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1173334Generated: November 2, 2026

1-(Benzyloxy)-3,5-di-tert-butyl-2-[2-nitrovinyl]benzene → 2-(2-Aminoethyl)-3,5-di-tert-butylphenol

https://huagongshe.com/reaction/1173334

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(Benzyloxy)-3,5-di-tert-butyl-2-[2-nitrovinyl]benzeneHCID 68717731—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product2-(2-Aminoethyl)-3,5-di-tert-butylphenolHCID 10060637—

Reaction Steps

To a solution of 0.183 g (0.5 mmol) of the product of Step B in 10 mL of methanol was added 0.1 g of 10% palladium on carbon catalyst and the reaction mixture was stirred in Parr shaker under 40 psig of hydrogen overnight. The reaction mixture was then filtered through Celite filter aid and the filtrate was evaporated in vacuo. The residue was purified on a silica gel flash chromatography column eluted with mixtures of CH2Cl2/MeOH/conc. NH4OH of the following compositions: 97/3/0.3; 95/5/0.5; and 90/10/1. Combination of the purified fractions and drying in vacuo afforded the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07834062B2
Source datasetuspto-grants-2010_11
ORD IDord-126995ba4c4742338c5c6678938d3072
Source noteuspto-grants-2010_11