HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrabutylammonium Fluoride → N-Boc-5-Hydroxyindole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | HCID 23398221 | HCID 23398221 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-Boc-5-Hydroxyindole | HCID 22596220 | — |
Reaction Steps
A solution (0.18 M) of tert-butyl 5-{[tert-butyl(dimethyl)silyl]oxy}-1H-indole-1-carboxylate in THF was treated with TBAF (1.1 eq) at 0° C. The mixture was stirred at that temperature for 10 min and allowed to reach room temperature. The reaction was quenched by the addition of saturated aqueous NH4Cl solution and extracted with ethyl acetate. The organic layer was washed with H2O, brine and dried over Na2SO4. The crude product was purified by column chromatography on silica gel (Petroleum ether:EtOAc 92/8) to afford the title compound as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07879815B2 |
| Source dataset | uspto-grants-2011_02 |
| ORD ID | ord-58aee2a7f5694d0ba50cfd67eb2d070b |
| Source note | uspto-grants-2011_02 |