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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1296012Generated: October 31, 2026

Ethyl acetate hexane → 1-[3-Amino-5-(tert-butyl)-4-hydroxyphenyl]-1-ethanone

https://huagongshe.com/reaction/1296012

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl acetate hexaneHCID 21226206—
Reactant1-[3-(Tert-butyl)-4-hydroxy-5-nitrophenyl]-1-ethanoneHCID 22929728—
CatalystHCID 178418390HCID 178418390—
SolventEthyl AcetateHCID 8857—
Product1-[3-Amino-5-(tert-butyl)-4-hydroxyphenyl]-1-ethanoneHCID 2292992671.8%

Reaction Steps

After adding 10% palladium-carbon (50% wet) (100 mg) to a solution of 1-[3-(tert-butyl)-4-hydroxy-5-nitrophenyl]-1-ethanone (1.00 g, 4.22 mmol) in ethyl acetate (10 ml) at room temperature, the mixture was hydrogenated for 3 hours under normal pressure. The 10% palladium-carbon was then filtered through celite and the solvent was distilled off under reduced pressure. The residue was subjected to silica gel chromatography (Wakogel-C200,10 g) to yield the title compound (627 mg, 71.8% yield) as a light red powder from the ethyl acetate-hexane (1:4˜1:3) fraction.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07244730B2
Source datasetuspto-grants-2007_07
ORD IDord-cf3fe3f1f67d42618a9bbc8908a96727
Source noteuspto-grants-2007_07