HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl acetate hexane → 1-[3-Amino-5-(tert-butyl)-4-hydroxyphenyl]-1-ethanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl acetate hexane | HCID 21226206 | — |
| Reactant | 1-[3-(Tert-butyl)-4-hydroxy-5-nitrophenyl]-1-ethanone | HCID 22929728 | — |
| Catalyst | HCID 178418390 | HCID 178418390 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 1-[3-Amino-5-(tert-butyl)-4-hydroxyphenyl]-1-ethanone | HCID 22929926 | 71.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07244730B2 |
| Source dataset | uspto-grants-2007_07 |
| ORD ID | ord-cf3fe3f1f67d42618a9bbc8908a96727 |
| Source note | uspto-grants-2007_07 |