HuagongsheHuagongshe Chemistry Print Report · For research reference only
Imidazole → 4-(t-Butyldimethylsilyloxy)indole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | tert-Butyldimethylsilyl chloride | HCID 28928 | — |
| Reactant | 1H-indol-4-ol | HCID 75421 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-(t-Butyldimethylsilyloxy)indole | HCID 11593976 | 100% |
Reaction Steps
A solution of 4-hydroxyindole (3.0 g, 22.5 mmol), t-butyldimethylsilyl chloride (5.09 g, 33.8 mmol) and imidazole (3.83 g, 56.3 mmol) in dimethylformamide (60 mL) was stirred at room temperature for 24 hours. Aqueous ammonium chloride was added (100 ml) and extracted several times with ethyl acetate. The organic layers were combined, dried over magnesium sulfate, and evaporated to give a crude oil. Flash chromatography (10% ethyl acetate/hexanes) yielded the desired product (5.55 g, 100%) as a white solid. NMR.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05840738 |
| Source dataset | uspto-grants-1998_11 |
| ORD ID | ord-7f76edcaf99d43afaf285435126d23bf |
| Source note | uspto-grants-1998_11 |