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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 365973Generated: October 25, 2026

2,4-Difluorobenzaldehyde → 2,4-Difluoro-1-methylbenzene

https://huagongshe.com/reaction/365973

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4-DifluorobenzaldehydeHCID 73770—
Reactant2,4-Difluorobenzyl alcoholHCID 91867—
CatalystNickelHCID 935—
Product2,4-Difluoro-1-methylbenzeneHCID 6798368.6%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06127581
Source datasetuspto-grants-2000_10
ORD IDord-7abb27e4324043f09f8c1963b7bffe45
Source noteuspto-grants-2000_10