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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3,5-Dimethyl-4-(3'-isopropyl-4'-benzyloxyphenoxy)-nitrobenzene | HCID 19030096 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | Heptane | HCID 8900 | — |
| Solvent | Tetrahydrofuran ethanol | HCID 21873804 | — |
| Product | 4-(4-Amino-2,6-dimethyl-phenoxy)-2-isopropyl-phenol | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05401772 |
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| Source dataset | uspto-grants-1995_03 |
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| ORD ID | ord-8d32b9ea51694687aab80516c66f8d8d |
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| Source note | uspto-grants-1995_03 |
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