HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 58020579, compound → 4-fluoro-1H-indol-5-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 58020579 | HCID 58020579 | — |
| Reactant | [5-(Benzyloxy)-4-fluoro-2-nitrophenyl]acetonitrile | HCID 58020678 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-fluoro-1H-indol-5-ol | HCID 22030553 | — |
| Product | 6-Fluoro-1H-indol-5-ol | HCID 22030929 | — |
Reaction Steps
A solution of a mixture of 3-cyanomethyl-2-fluoro-4-nitrobenzyloxybenzene and 5-cyanomethyl-2-fluoro-4-nitrobenzyloxybenzene (23 g, 80.4 mmol) in ethanol (220 ml) and acetic acid (30 ml) containing 10% palladium on charcoal (600 mg) was hydrogenated under 3 atmospheres pressure until hydrogen uptake ceased. The mixture was filtered and the filtrate was evaporated under vacuum. The residue was purified on column chromatography using a Prochrom® equipment eluting with methylene chloride/petroleum ether (20/80) to give 4-fluoro-5-hydroxyindole (2.48 g) and 6-fluoro-5-hydroxyindole (3.5 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08492560B2 |
| Source dataset | uspto-grants-2013_07 |
| ORD ID | ord-98e6b66d0071416dbffc5158c271e1e8 |
| Source note | uspto-grants-2013_07 |