Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1836551Generated: November 3, 2026

{4-(Benzyloxy)-3-[(4-fluorophenyl)sulphonyl]phenyl}methanol → 4-(Benzyloxy)-3-[(4-fluorophenyl)sulphonyl]benzaldehyde

https://huagongshe.com/reaction/1836551

Reaction equation

Participants

RoleNameHCIDCharge
Reactant{4-(Benzyloxy)-3-[(4-fluorophenyl)sulphonyl]phenyl}methanolHCID 23499600—
CatalystHCID 178418406HCID 178418406—
SolventDichloromethaneHCID 6344—
Product4-(Benzyloxy)-3-[(4-fluorophenyl)sulphonyl]benzaldehydeHCID 23499592—

Reaction Steps

2.1 g (5.64 mmol) of {4-(benzyloxy)-3-[(4-fluorophenyl)sulphonyl]phenyl}methanol (Example V) are dissolved in 25 ml of dichloromethane. At room temperature, 4.9 g (56.39 mmol) of manganese(IV) oxide are added. The mixture is stirred at room temperature overnight. The reaction mixture is then filtered through Celite and the solvent is removed under reduced pressure. This gives 1.82 g (86% of theory) of 4-(benzyloxy)-3-[(4-fluorophenyl)sulphonyl]benzaldehyde.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06777442B2
Source datasetuspto-grants-2004_08
ORD IDord-f49d8ed7679a451aa4d97acb07ce86c0
Source noteuspto-grants-2004_08