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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1609736Generated: October 30, 2026

3,5-Dimethyl-4-(3'-isopropyl-4'-benzyloxyphenoxy)-nitrobenzene → 4-(4-Amino-2,6-dimethyl-phenoxy)-2-isopropyl-phenol

https://huagongshe.com/reaction/1609736

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,5-Dimethyl-4-(3'-isopropyl-4'-benzyloxyphenoxy)-nitrobenzeneHCID 19030096—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthyl AcetateHCID 8857—
SolventHeptaneHCID 8900—
SolventTetrahydrofuran ethanolHCID 21873804—
Product4-(4-Amino-2,6-dimethyl-phenoxy)-2-isopropyl-phenolHCID 12114179—

Reaction Steps

3,5-Dimethyl-4-(3'-isopropyl-4'-benzyloxyphenoxy)-nitrobenzene, (2.86 kg, 7.31 mol) is dissolved in a mixture of ethanol/tetrahydrofuran (10:1, 114L) and cooled to 10°. This is admixed with 10% Pd/C (800g) and the system is pressurized to 15 psi with hydrogen gas. The hydrogenation is continued for 18 hours. The mixture is then filtered through Celite and the Celite is washed with tetrahydrofuran (30 L). The filtrate is then evaporated in vacuo to dryness (50°, 3 Torr). The solid residue is triturated with heptane (3L) and filtered. The filter cake is washed with heptane (2×500 mL) to obtain crude product which is then dissolved in hot ethyl acetate (14 L) and diluted with heptane (30 L). The product slowly precipitates and the mixture is cooled at 10°for 1 hour, collected by filtration and washed with ethyl acetate/hexane 1:2 (2×500 mL). The filter cake is then dried (60°, 3 Torr) for 24 hours to yield 3,5-dimethyl4-(3'-isopropyl-4'-hydroxyphenoxy)-aniline, m.p. 180°-181°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05401772
Source datasetuspto-grants-1995_03
ORD IDord-8d32b9ea51694687aab80516c66f8d8d
Source noteuspto-grants-1995_03