HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-allyl-5-hydroxy-N-(4-chlorophenyl)indole → 5-hydroxy-4-propyl-N-(4-chlorophenyl)indole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-allyl-5-hydroxy-N-(4-chlorophenyl)indole | HCID 54126383 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 5-hydroxy-4-propyl-N-(4-chlorophenyl)indole | HCID 53747016 | — |
Reaction Steps
4-allyl-5-hydroxy-N-(4-chlorophenyl)indole (Step C; 1.0 g, 3.54 mmol) was taken up in 25 mL ethyl acetate and hydrogenated (1 atm) at ambient temperature using 5% palladium on charcoal (40 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-7539911006f84abd9c786bc8d010741f |
| Source note | uspto-grants-1999_01 |