HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-allyl-5-hydroxy-N-(4-fluorobenzyl)indole → 4-propyl-5-hydroxy-N-(4-fluorobenzyl)indole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-allyl-5-hydroxy-N-(4-fluorobenzyl)indole | HCID 53978806 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4-propyl-5-hydroxy-N-(4-fluorobenzyl)indole | HCID 53701199 | — |
Reaction Steps
4-allyl-5-hydroxy-N-(4-fluorobenzyl)indole (Step C; 0.40 g, 1.42 mmol) was taken up in 10 mL ethyl acetate and hydrogenated (1 atm) at ambient temperature using 5% palladium on charcoal (15 mg) for 2 hours. The reaction was filtered through celite and concentrated in vacuo to provide the title compound which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05859051 |
| Source dataset | uspto-grants-1999_01 |
| ORD ID | ord-9aff132308f947809bee9000b430f7ab |
| Source note | uspto-grants-1999_01 |