HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydride → 5-allyloxy-N-neopentylindole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Propane, 1-iodo-2,2-dimethyl- | HCID 84953 | — |
| Reactant | 5-(prop-2-en-1-yloxy)-1H-indole | HCID 14239230 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-allyloxy-N-neopentylindole | HCID 18672460 | — |
Reaction Steps
To a solution of sodium hydride (60%, 254 mg, 6.35 mmol) in 15 mL tetrahydrofuran (THF) was added 5-allyloxyindole (Step A; 1.0 g, 5.77 mmol) in 5 mL THF and the mixture was stirred for 1 hour at ambient temperature. Neopentyl iodide (0.69 mL, 6.35 mmol) was added and the reaction heated to reflux for 21 hours. After cooling, the reaction was quenched with saturated aqueous ammonium chloride and extracted with ethyl acetate. The organic layer was washed with water, brine, dried over magnesium sulfate, filtered, concentrated in vacuo, and the crude residue purified by flash chromatography on silica gel (15% ethyl acetate/hexane) to provide the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06160000 |
| Source dataset | uspto-grants-2000_12 |
| ORD ID | ord-8d4340160ff04dc793a528bdda82125c |
| Source note | uspto-grants-2000_12 |