HuagongsheHuagongshe Chemistry Print Report · For research reference only
Propylene Oxide → (6-Benzyloxy-indol-1-yl)-propan-2-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Propylene Oxide | HCID 6378 | — |
| Reactant | 6-(benzyloxy)-1H-indole | HCID 260804 | — |
| Product | (6-Benzyloxy-indol-1-yl)-propan-2-ol | HCID 22247173 | — |
Reaction Steps
6-Benzyloxyindole (1) (Batcho and Leimgruber, Organic Syntheses, Collective Vol. 7, p. 34 (1990)) is reacted with (±)-propylene oxide and a base in an organic solvent to yield (±)-1-(2-hydroxypropyl)-6-benzyloxyindole (2). Preferably the base is sodium hydride and the solvent is tetrahydrofuran. The temperature is 0° C. to 25° C., preferably about 10° C. Preferably an inert atmosphere, e.g., nitrogen or argon, is maintained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06998489B2 |
| Source dataset | uspto-grants-2006_02 |
| ORD ID | ord-c9269fc643d04eaf8aacfbc51d040769 |
| Source note | uspto-grants-2006_02 |