HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1072585Generated: October 25, 2026
Ethanol → 2-Methyl-1-[7-(benzyloxy)indol-3-yl]prop-2-ylamine
https://huagongshe.com/reaction/1072585
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | 3-(2-Methyl-2-nitropropyl)-7-(benzyloxy)indole | HCID 22014778 | — |
| Catalyst | Nickel | HCID 935 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Methyl-1-[7-(benzyloxy)indol-3-yl]prop-2-ylamine | HCID 22014779 | — |
Reaction Steps
A mixture of 3-(2-methyl-2-nitropropyl)-7-(benzyloxy)indole (25.0 g, 77.1 mmol), Raney Nickel® (9.5 g wet lump), and 3A ethanol (250 mL) is pressurized to 50 psig with H2 and is heated to 60° C. After 1 hour, the mixture is cooled to ambient temperature. The mixture is diluted with tetrahydrofuran (100 mL) and is warmed to 50° C. The catalyst is removed by filtration and the cake is rinsed with 50° C. tetrahydrofuran (4×50 mL). The filtrate is concentrated to a solid which is dried in a 50° C. vacuum oven to provide 22.41 (99%) of 2-methyl-1-[7-(benzyloxy)indol-3-yl]prop-2-ylamine. MS (ES+) m/z 295 (100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06911463B2 |
|---|
| Source dataset | uspto-grants-2005_06 |
|---|
| ORD ID | ord-7673ff0e0e814ed6855012d5c2b2b855 |
|---|
| Source note | uspto-grants-2005_06 |
|---|