HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Alcohol → HCID 86665019, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Alcohol | HCID 244 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 8-Bromo-6-chloroimidazo(1,2-b)pyridazine | HCID 46835269 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86665019 | HCID 86665019 | — |
Reaction Steps
To a stirred solution of phenylmethanol (3.35 g, 31 mmol, 1.2 eq) in THF (80 mL), NaH (60% dispersion in mineral oil, 1.34 g, 33.5 mmol, 1.3 eq) is added in portions. The resulting mixture is stirred at RT for 30 min and then 8-bromo-6-chloroimidazo[1,2-b]pyridazine (D-3) (6 g, 25.8 mmol, 1.0 eq) is added. The resulting mixture is stirred at RT for an additional 2 h and then poured into water (30 mL). The mixture is extracted with ethyl acetate (2×100 mL). The combined organic layers are washed with brine, dried over Na2SO4 and filtered. The filtrate is concentrated in vacuo to afford the product, 8-(benzyloxy)-6-chloroimidazo[1,2-b]pyridazine (D-4).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08901133B2 |
| Source dataset | uspto-grants-2014_12 |
| ORD ID | ord-3d3c480f43114507ae186badd6e0c19d |
| Source note | uspto-grants-2014_12 |