Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Triphenylcarbinol | HCID 6457 | — |
| Reactant | 2-sec-Butylphenol | HCID 6984 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 90021602 | HCID 90021602 | 75% |
Reaction Steps
A 250 mL 1-neck flask was equipped with a magnetic stirrer and a reflux condenser with nitrogen blanket. The flask was charged with 6.52 grams (0.025 moles) of trityl alcohol, 3.77 grams (0.025 moles) of o-sec-butylphenol, and 50 mL of glacial acetic acid. The mixture was stirred under nitrogen at room temperature to give a clear, yellow solution. Concentrated sulfuric acid (5 mL) was then added in one portion. The solution immediately became dark red-brown. The solution was stirred at room temperature for 2 days, during which time solids separated out. The reaction mixture was filtered, and the solids were washed on the filter with several portions of water. After drying in a vacuum oven at 65° C. for 3 hours, the yield of product was 7.34 grams (75% yield). MP=135-136° C. GPC analysis showed a purity of >99%. The structure was confirmed by IR, 1H- and 13C-NMR analyses.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09422493B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-bb647d37360c49438bf4d08f91a663fa |
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| Source note | uspto-grants-2016_08 |
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