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 shown in the following Scheme, hydroquinone (1) (4.5 g (grams)) and 1,6-dibromo hexane (2) (10 g (grams)) were dissolved in methanol (100 ml (milliliters)) at a room temperature. Potassium hydroxide (2.3 g (grams)) was added to the resulting mixture solution, and then fluxed at 60° C. (Celsius) overnight. Next day, the temperature of the reaction mixture is lowered to a room temperature, and methanol was evaporated from the reaction mixture. Then, the reaction mixture was extracted three times with water (100 ml (milliliters)) and ethyl acetate (100 ml (milliliters)). Water was removed over magnesium sulfate, and the solvents were evaporated, and the resulting reaction mixture was purified using a column chromatography (developer solution: ethylacetate/hexane=1/5 volume ratio) to obtain 4.4 g (grams) of 4-(6-bromohexyloxy)phenol (3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08545717B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-87ba805f1ada4c0cb0c7fe7447ad93d2 |
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| Source note | uspto-grants-2013_10 |
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