HuagongsheHuagongshe Chemistry Print Report · For research reference only
Boronic Acid → 6-Phenylnaphtho[2,1-b]benzofuran
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Boronic Acid | HCID 61668 | — |
| Reactant | Benzo(b)naphtho(1,2-d)furan | HCID 268932 | — |
| Product | 6-Phenylnaphtho[2,1-b]benzofuran | HCID 67980454 | — |
Reaction Steps
In this reference example, a position was specified where the benzo[b]naphtho[1,2-d]furan which was synthesized as an intermediate in each of Synthesis Example 1 and Synthesis Example 2 was converted into boronic acid in the reaction scheme (E1-3). Specifically, 6-phenylbenzo[b]naphtho[1,2-d]furan (abbreviation: PBnf) was synthesized using the compound synthesized in the reaction scheme (E1-3), and was subjected to X-ray crystallography.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08674117B2 |
| Source dataset | uspto-grants-2014_03 |
| ORD ID | ord-262375e5fb2048e990e785b6701dc605 |
| Source note | uspto-grants-2014_03 |