Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thiophenol | HCID 7969 | — |
| Reactant | HCID 21518032 | HCID 21518032 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 136354596 | HCID 136354596 | — |
Reaction Steps
15g of 2-(1-phenyl-5-tetrazolylthio)-6-(1,1,3,3-tetramethylbutyl)-p-benzoquinone was added to 150ml of methanol and the mixture was cooled to 0°C while stirring. Then a solution of 4.5g of thiophenol in 25ml of methanol was added dropwise to this mixture. After the addition, the mixture was stirred at 0°C for 3 hours. The resulting crystals were separated by filtration and recrystallized from a solvent mixture of n-hexane and ethyl acetate (n-hexane/ethyl acetate = 5/1 by volume). Thus 7.5g of 2-(1-phenyl-5-tetrazolylthio)-3-phenylthio-6-(1,1,3,3-tetramethylbutyl)-hydroquinone having a melting point of 147°C was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03975395 |
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| Source dataset | uspto-grants-1976_08 |
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| ORD ID | ord-42b2c56145794b0f86b28a481405fd16 |
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| Source note | uspto-grants-1976_08 |
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