HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Phenoxyphenylboronic acid → 5-(tert-Butyl)-2-hydroxy-4'-phenoxy-[1,1'-biphenyl]-3-carbaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Phenoxyphenylboronic acid | HCID 2734377 | — |
| Reactant | 3-Bromo-5-tert-butyl-2-hydroxybenzaldehyde | HCID 7172096 | — |
| Reactant | 5-(Tert-butyl)-2-hydroxy-4'-(trifluoromethoxy)-[1,1'-biphenyl]-3-carbaldehyde | HCID 86718719 | — |
| Product | 5-(tert-Butyl)-2-hydroxy-4'-phenoxy-[1,1'-biphenyl]-3-carbaldehyde | HCID 86718720 | — |
Reaction Steps
5-(tert-Butyl)-2-hydroxy-4′-phenoxy-[1,1′-biphenyl]-3-carbaldehyde was prepared as an orange oil using the procedure described in Intermediate 5 from 3-bromo-5-(tert-butyl)-2-hydroxybenzaldehyde (Intermediate 4) and 4-phenoxyphenylboronic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09296696B2 |
| Source dataset | uspto-grants-2016_03 |
| ORD ID | ord-8a56cd6f4170443ea25ffa5a70b98332 |
| Source note | uspto-grants-2016_03 |