HuagongsheHuagongshe Chemistry Print Report · For research reference only
(4-Pentylphenyl)boronic acid → 3,4-Difluoro-4'-pentylbiphenyl-2-carbaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (4-Pentylphenyl)boronic acid | HCID 4589191 | — |
| Reactant | 6-Bromo-2,3-difluorobenzaldehyde | HCID 9877851 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Product | 3,4-Difluoro-4'-pentylbiphenyl-2-carbaldehyde | HCID 22644333 | — |
Reaction Steps
2-bromo-5,6-difluorobenzaldehyde is reacted with 4-pentylphenylboronic acid in the presence of a Pd catalyst to give 3,4-difluoro-4′-pentylbiphenyl-2-carbaldehyde. This compound is reacted with trimethylsulfonium iodide, to give 3,4-difluoro-2-(oxiran-2-yl)-4′-pentyl-biphenyl. Without further purification, this compound is converted into 1,2-difluoro-7-pentylphenanthrene in the presence of BF3 etherate. The raw product is purified by the procedure typical for this type of liquid-crystal materials (cf. DE-A 195 00 768), yielding 1,2-difluoro-7-pentylphenanthrene in the form of colorless crystals. Kumar, J. Org. Chem. 1997, 62, 8535-8539 discloses the coupling of boronic acid compounds with a bromo compound having aldehyde functionality.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06811832B2 |
| Source dataset | uspto-grants-2004_11 |
| ORD ID | ord-d904689d8ca44f2aa25e9f012d384d67 |
| Source note | uspto-grants-2004_11 |