HuagongsheHuagongshe Chemistry Print Report · For research reference only
Aluminium lithium hydride → 2-(Benzyloxy)-4,5,6,7-tetrahydropyrazolo[1,5-a]pyrazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | 2-(benzyloxy)-6,7-dihydropyrazolo[1,5-a]pyrazin-4(5H)-one | HCID 72714787 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-(Benzyloxy)-4,5,6,7-tetrahydropyrazolo[1,5-a]pyrazine | HCID 86706492 | 97% |
Reaction Steps
A 1 M solution of lithium aluminum hydride in THF (0.77 mL, 0.77 mmol) was added dropwise to a stirred solution of 2-(benzyloxy)-6,7-dihydropyrazolo[1,5-a]pyrazin-4(5H)-one (0.16 g, 0.65 mmol) in THF (4 mL) under nitrogen at 0° C. The mixture was stirred at room temperature for 4 hours and diluted with AcOEt. Na2SO4.10H2O was added at 0° C. and the mixture was stirred for 20 minutes at this temperature, filtered through a pad of diatomaceous earth and then washed with additional AcOEt. The filtrate was evaporated in vacuo to yield 2-(benzyloxy)-4,5,6,7-tetrahydropyrazolo[1,5-a]pyrazine (0.14 g, 97% yield) as a yellow oil, that was used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09029366B2 |
| Source dataset | uspto-grants-2015_05 |
| ORD ID | ord-35b5b4aca22642f1a997a14a3f48b21c |
| Source note | uspto-grants-2015_05 |