Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl Alcohol | HCID 244 | — |
| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Sodium Bromide | HCID 253881 | — |
| Catalyst | Cobalt(II) acetate tetrahydrate | HCID 61372 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | Benzaldehyde | HCID 240 | 50.2% |
| Product | Benzoic Acid | HCID 243 | 48.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05473101 |
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| Source dataset | uspto-grants-1995_12 |
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| ORD ID | ord-45ad7edd32904de48cfe27fdbae542bf |
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| Source note | uspto-grants-1995_12 |
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