Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydroquinone | HCID 785 | — |
| Reactant | 1,6-Dibromohexane | HCID 12368 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 19894591 | HCID 19894591 | 39.4% |
Reaction Steps
As expressed in the following reaction scheme, hydroquinone (1) (4.5 g) and 1,6-dibromo hexane (2) (10 g) were dissolved in methanol (100 ml) at room temperature. Potassium hydroxide (2.3 g) was added to the mixture solution, and the resulting solution was then refluxed at 60° C. overnight. Then, the resulting reaction mixture is cooled to room temperature, and methanol was removed from the reaction mixture through evaporation, and the product was then extracted three times with water (100 ml) and ethyl acetate (100 ml)(200 ml×3). After removing water with magnesium sulfate and evaporating the solvent, the reaction product was refined by column chromatography (eluent: ethyl acetate/hexane=1/5) to obtain 4.4 g of 4-(6-bromohexyloxy)phenol (3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08465671B2 |
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| Source dataset | uspto-grants-2013_06 |
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| ORD ID | ord-09409d5122304e108edc98fb5774b01d |
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| Source note | uspto-grants-2013_06 |
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