Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methylhydroquinone | HCID 7253 | — |
| Reactant | Trimethylhydroquinone | HCID 12785 | — |
| Reactant | 2,3-Dimethylhydroquinone | HCID 69100 | — |
| Catalyst | Iron | HCID 23925 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Durohydroquinone | HCID 136346 | — |
Reaction Steps
Into an autoclave (inner volume: 9 ml, made of SUS 316, equipped with a manometer) were charged 0.104 g of methylhydroquinone, 3.4078 g of methanol and 8.3 mg of iron powders (manufactured by Wako Pure Chemical Ind., Ltd.). The reaction was started by elevating the temperature up to 350° C. with sand bath. The pressure during the reaction was 20 MPa. After 2 hours, the autoclave was quickly cooled and the reaction solution was taken out from the autoclave when the temperature was cooled back to the room temperature. The measurement according to the process described above revealed that the conversion of methylhydroquinone was 16% by mole, the selectivity of dimethylhydroquinone was 82% by mole and the selectivity of trimethylhydroquinone was 3% by mole. No tetramethylhydroquinone was produced.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06303801B1 |
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| Source dataset | uspto-grants-2001_10 |
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| ORD ID | ord-af2687bb1220432cb1ed01fbda9f5006 |
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| Source note | uspto-grants-2001_10 |
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