HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,4-Difluorobenzaldehyde → 2,4-Difluoro-1-methylbenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,4-Difluorobenzaldehyde | HCID 73770 | — |
| Reactant | 2,4-Difluorobenzyl alcohol | HCID 91867 | — |
| Catalyst | Nickel | HCID 935 | — |
| Product | 2,4-Difluoro-1-methylbenzene | HCID 67983 | 68.6% |
Reaction Steps
DE-A 2,333,849 discloses that 2,4-difluorobenzaldehyde can be converted into 2,4-difluorobenzyl alcohol in a yield of 68.6% by hydrogenation over Raney nickel. Disadvantages of this process are not only the large amount of catalyst (31 g per mol) and the large amount of a solvent (1100 ml per mole) but also the unsatisfactory yield of 68.6%. These factors result in an unsatisfactory space-time yield. The aldehyde used was obtained here from the difficult-to-obtain 2,4-difluorotoluene by side-chain chlorination and subsequent hydrolysis.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06127581 |
| Source dataset | uspto-grants-2000_10 |
| ORD ID | ord-7abb27e4324043f09f8c1963b7bffe45 |
| Source note | uspto-grants-2000_10 |