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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2259467Generated: November 4, 2026

Benzyl Alcohol → Benzaldehyde

https://huagongshe.com/reaction/2259467

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
ReactantHydrogen PeroxideHCID 784—
ReactantSodium BromideHCID 253881—
CatalystCobalt(II) acetate tetrahydrateHCID 61372—
SolventAcetic AcidHCID 176—
ProductBenzaldehydeHCID 24050.2%
ProductBenzoic AcidHCID 24348.8%

Reaction Conditions

Temperature80 °C

Reaction Steps

Cobalt (II) acetate tetrahydrate (0.5 g, 0.002 moles), sodium bromide (0.5 g, 0.005 moles), benzyl alcohol (2.93 g, 0.027 moles) and acetic acid (25 g) were charged to a vessel fitted with a overhead paddle stirrer, thermometer and condenser and heated to 80° C. Hydrogen peroxide (30%, 0.22 moles) was added dropwise down the condenser over two hours during which time the reaction mixture changed colour from deep blue to pink. The reaction was continued for a further 90 minutes after which it was stopped and analysed by HPLC. The analysis revealed that 99.0% of the benzyl alcohol had been consumed, yielding products including benzaldehyde (50.2% yield) and benzoic acid (48.8% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05473101
Source datasetuspto-grants-1995_12
ORD IDord-45ad7edd32904de48cfe27fdbae542bf
Source noteuspto-grants-1995_12