HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-(Tributylstannyl)methanol → HCID 21220903, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(Tributylstannyl)methanol | HCID 4193593 | — |
| Reactant | 5-Bromo-1-benzofuran-7-carbaldehyde | HCID 21220840 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 21220903 | HCID 21220903 | 60.1% |
Reaction Steps
A mixture of 5-bromo-benzofuran-7-carbaldehyde (2.02 g), hydroxymethyltributyltin (4.29 g) and tetrakis(triphenylphosphine palladium (O) (1.03 g) in dry 1,4-dioxan (8 ml) was heated at reflux for 18 h. A further portion of catalyst (203 mg) was added and heating continued for 4 h. The reaction mixture was allowed to cool, and the solution was purified by FCC eluted with hexane:ethyl acetate (1:1) to give the title compound as yellow oil (0.95 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05935972 |
| Source dataset | uspto-grants-1999_08 |
| ORD ID | ord-82ede1bd2c714345a3a9ffaa9d90ed3e |
| Source note | uspto-grants-1999_08 |