Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formic Acid | HCID 284 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | Lithium Carbonate | HCID 11125 | — |
| Reactant | 2,4-Di-tert-butylphenyl methanesulfonate | HCID 44542716 | — |
| Catalyst | HCID 178418390 | HCID 178418390 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1,3-Di-tert-butylbenzene | HCID 136810 | 95.5% |
Reaction Steps
In a nitrogen atmosphere under normal pressure, 2,4-di-tert-butylphenyl methanesulfonate (30 g, 0.11 mols), formic acid (9.7 g, 0.21 mols), lithium carbonate (7.8 g, 0.11 mols) and methanol (180 g) were mixed at 25° C., and with stirring, 10 mass % Pd/carbon (50 mass % water-containing product) (6 g) (as metal palladium; 1 mass % relative to 2,4-di-tert-butylphenyl methanesulfonate) as supported by a carbon carrier having a specific surface area of 780 m2/g (by BET method) was put into it. With stirring, the reaction liquid was reacted at the same temperature for 4 hours. Water (10 mL) was added to the reaction liquid and Pd-carbon was separated through filtration, then heptane (30 g) was added to the filtrate. The organic layer obtained after extraction was concentrated under reduced pressure to give crude 1,3-di-tert-butylbenzene (20 g, yield 100% by mass). The result is shown in Table II-2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08283508B2 |
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| Source dataset | uspto-grants-2012_10 |
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| ORD ID | ord-5982644b64a349c1a477c92f55b4dfa0 |
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| Source note | uspto-grants-2012_10 |
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