Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | 1-Bromopentane | HCID 8057 | — |
| Reactant | 3,5-Dibromophenol | HCID 12280 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Catalyst | Benzyltributylammonium chloride | HCID 159952 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1,3-Dibromo-5-isobutoxybenzene | HCID 50852773 | — |
Reaction Steps
Potassium hydroxide (15.9 g; 284 mmol) was dissolved in water (300 ml) and 3,5-dibromo-phenol (47 g; 188.5 mmol) was added. Benzyl tributylammoniumchloride (17.7 g; 56.8 mmol) and toluene (200 ml) was added and the reaction mixture was heated to 85° C. Bromoethylpropan (32.3 g; 325.7 mmol) was added over 5 hours and the reaction mixture was stirred at 85° C. for additional 16 h. The reaction mixture was cooled to room temperature and the phases were separated. Toluene (100 ml) was added to the organic phase which was washed with 0.2 N aqueous HCl (200 ml×2) and water (200 ml×2). The organic phase was evaporated to give the crude product which was purified by distillation (0.7. mm Hg; Bp: 98° C.); Yield: 43 g (colourless oil).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07943669B2 |
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| Source dataset | uspto-grants-2011_05 |
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| ORD ID | ord-ac940c3642d141a3856e88566bfa9c7d |
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| Source note | uspto-grants-2011_05 |
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