HuagongsheHuagongshe Chemistry Print Report · For research reference only
Homoallyl bromide → HCID 178450298, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Homoallyl bromide | HCID 21241 | — |
| Reactant | HCID 57548087 | HCID 57548087 | — |
| Reactant | HCID 178420268 | HCID 178420268 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 178450298 | HCID 178450298 | 43% |
Reaction Steps
Compound 32D was prepared following the procedure as described for the synthesis of compound 32A (see Scheme 5) using 4-bromo-but-1-ene as the alkyl halogenide and 3-pyridin-3-yl-1-(2-trimethylsilanyl-1-ethoxymethyl)-1H-pyrazol-4-ol (30). Work-up and flash chromatography (diethyl ether) afforded compound 31 D. Yield 43% (oil, TLC diethyl ether Rf 0.37), which was subsequently deprotected (TBAF/THF) to afford 3-(4-but-3-enyloxy-1H-pyrazol-3-yl)-pyridine (32D).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08084473B2 |
| Source dataset | uspto-grants-2011_12 |
| ORD ID | ord-f982a84d99ef4665b65ce44e56962f74 |
| Source note | uspto-grants-2011_12 |