Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Toluene | HCID 1140 | — |
| Reactant | 1-Hexadecyl-4-methoxybenzene | HCID 14143934 | — |
| Catalyst | Hexadecyltributylphosphonium bromide | HCID 84716 | — |
| Solvent | Water | HCID 962 | — |
| Product | Phenol, 4-hexadecyl- | HCID 75768 | — |
Reaction Steps
The alkyl anisole of Example 1 (40 g) was transferred to a dry 3-neck 1-litre flask under nitrogen. To this was added tributylhexadecylphosphonium bromide (12.69 g) and HBr (48% aq., 71.4 ml). The resulting thick suspension was warmed to 135° C. and stirred for five hours. Toluene was added and the reaction was transferred to a separating funnel. The organic layer was shaken with water and then the aqueous extract shaken with fresh toluene. The organic extracts were combined and dried with MgSO4. The solvent was removed in vacuo to give the title compound as a brown solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08404627B2 |
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| Source dataset | uspto-grants-2013_03 |
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| ORD ID | ord-561e088031d9415eabe5d14cf3b3d33b |
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| Source note | uspto-grants-2013_03 |
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