HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Fluoro-2-nitro-1-propoxybenzene → 5-Fluoro-2-propoxyaniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Fluoro-2-nitro-1-propoxybenzene | HCID 66917174 | — |
| Catalyst | HCID 178418390 | HCID 178418390 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 5-Fluoro-2-propoxyaniline | HCID 26189633 | 86% |
Reaction Steps
4-Fluoro-2-nitro-1-propoxybenzene (2.0 g, 10.0 mmol) and 5% palladium carbon (750 mg) were added to ethanol (30 ml). Catalytic reduction was conducted at room temperature and atmospheric pressure (normal pressure). The catalyst was removed by celite filtration, and the filtrate was concentrated under reduced pressure. The residue was dissolved in dichloromethane, and dried over anhydrous magnesium sulfate. The resulting dry product was concentrated under reduced pressure to thereby obtain 1.45 g of oily red orange 5-fluoro-2-propoxyaniline (yield: 86%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09045464B2 |
| Source dataset | uspto-grants-2015_06 |
| ORD ID | ord-d7faf677e2ee4ac080ffcec65e377450 |
| Source note | uspto-grants-2015_06 |