Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Oxygen | HCID 977 | — |
| Reactant | 4-tert-Butyltoluene | HCID 7390 | — |
| Reactant | 4-tert-Butylbenzoic acid | HCID 7403 | — |
| Reactant | 1,3,5-Trihydroxy-1,3,5-triazinane-2,4,6-trione | HCID 10419723 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 4-tert-Butylbenzaldehyde | HCID 70324 | — |
Reaction Steps
In 3 mL of acetic acid was dissolved 315 mg of p-t-butyltoluene to give a solution, and the solution was combined with 156 mg of the catalyst C and 42 mg of hexahydro-1,3,5-trihydroxy-1,3,5-triazine-2,4,6-trione (hereinafter also referred to as “THICA”), followed by stirring at 100° C. in an oxygen atmosphere for 6 hours. The reaction mixture was analyzed through gas chromatography to find that p-t-butylbenzoic acid and p-t-butylbenzaldehyde were produced in yields of 84.5% and 1.4%, respectively, with a conversion from p-t-butyltoluene of 99.7%. The catalyst C was separated from the reaction mixture through filtration, washed with ethyl acetate two times, dried at room temperature (25° C.) under reduced pressure, and thereby recovered as a catalyst C1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08410308B2 |
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| Source dataset | uspto-grants-2013_04 |
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| ORD ID | ord-48c3cc297a274581904be5fd07951a7d |
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| Source note | uspto-grants-2013_04 |
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