HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenylboronic Acid → 2-Fluoro-4-phenylbenzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenylboronic Acid | HCID 66827 | — |
| Reactant | 4-Bromo-2-fluorobenzaldehyde | HCID 143517 | — |
| Product | 2-Fluoro-4-phenylbenzaldehyde | HCID 16768527 | — |
Reaction Steps
The title compound was prepared in a similar manner to that described in Reference Example 2 using 4-bromo-2-fluoro-benzaldehyde instead of tert-butyl N-(4-bromobenzyl)carbamate and phenylboronic acid instead of 3-benzyloxyphenylboronic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07795236B2 |
| Source dataset | uspto-grants-2010_09 |
| ORD ID | ord-c4321426f7b24bf6b6e58373ddac92b8 |
| Source note | uspto-grants-2010_09 |