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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1109677Generated: October 27, 2026

1,3-Bis[4-(4-nitro-6-fluorophenoxy)-alpha, alpha-dimethylbenzyl]benzene → 1,3-Bis[4-(4-amino-6-fluorophenoxy)-alpha, alpha-dimethylbenzyl]benzene

https://huagongshe.com/reaction/1109677

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-Bis[4-(4-nitro-6-fluorophenoxy)-alpha, alpha-dimethylbenzyl]benzeneHCID 86747917—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventIsopropanolHCID 3776—
Product1,3-Bis[4-(4-amino-6-fluorophenoxy)-alpha, alpha-dimethylbenzyl]benzeneHCID 2259863481%

Reaction Steps

Successively, to a reduction vessel equipped with a thermometer, reflux condenser and stirrer, 115 g (0.184 mol) of 1,3-bis[4-(4-nitro-6-fluorophenoxy)-α, α-dimethylbenzyl]benzene, 250 g of isopropyl alcohol and 4.8 g of 5%-Pd/c having a moisture content of 50% were charged and reacted at 70°~80° C. for 4 hours in a hydrogen atmosphere. After finishing the reaction, the catalyst was filtered off and the filtrate was concentrated under reduced pressure to obtain 84.2 g (81% yield) of 1,3-bis[4-(4-amino-6-fluorophenoxy)-α, α-dimethylbenzyl]benzene as a light yellow crystal having a melting point of 130.4~132.9.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05321096
Source datasetuspto-grants-1994_06
ORD IDord-23daf556b28d401ab1dae3c4c46bba2c
Source noteuspto-grants-1994_06