Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 2,6-Di-t-butyl-p-benzoquinone | HCID 12867 | — |
| Reactant | Sodium Dithionite | HCID 24489 | — |
| Catalyst | Benzyl triethylammonium chloride | HCID 66133 | — |
| Solvent | Cyclohexane | HCID 8078 | — |
| Product | 2,6-Di-tert-butylhydroquinone | HCID 75550 | — |
Reaction Steps
To 1.2 L of water, 223.2 g (1.09 mol) of sodium hydrosulfite, 1.0 L of cyclohexane, 200.0 g (908 mmol) of 2,6-di-tert-butyl-1,4-benzoquinone and 20.7 g (90.9 mmol) of benzyltriethylammonium chloride were added and the mixture was stirred for 1 hour at 40° C. The reaction mixture was subjected to liquid-liquid separation and the aqueous layer was discarded. The organic layer was washed with 400 mL of water to give a solution of 2,6-di-tert-butylhydroquinone in cyclohexane.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06852867B2 |
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| Source dataset | uspto-grants-2005_02 |
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| ORD ID | ord-1a7183a29f1a46b5bbd54f46e3d145dc |
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| Source note | uspto-grants-2005_02 |
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