Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Butyl bromide | HCID 8002 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Methyl Syringate | HCID 70164 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Butyl ether | HCID 8909 | — |
Reaction Steps
A mixture of methyl 3,5-dimethoxy-4-hydroxybenzoate represented by Formula 87 (5 g, 23.56 mmol), 1-bromobutane (2.80 mL, 25.92 mmol), potassium carbonate (3.58 mg, 25.92 mmol) and potassium iodide (547.60 mg, 3.30 mmol) in DMF (50 mL) was agitated at 80° C. for 24 hours. After decreasing a temperature of the reaction mixture to room temperature, removing solids through filtration and adding ethyl acetate to the remaining filtrate, the filtrate was consecutively washed with water and a 5N-hydrochloric acid solution. After separating an organic layer and drying the same with magnesium sulfate, the solvent was removed under reduced pressure to form a concentrate mixture, which in turn, was subjected to separation and purification through column chromatography (ethyl acetate/hexane, 1:5) using silica gel (SiO2), resulting in an n-butylether compound represented by Formula 92 as a desired product (6.20 g, 94%). Analysis data of the product is provided as follows:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09359346B2 |
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| Source dataset | uspto-grants-2016_06 |
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| ORD ID | ord-ed6bc36895454f499aaa855841f115da |
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| Source note | uspto-grants-2016_06 |
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