Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Phenoxyphenol | HCID 13254 | — |
| Reactant | 2-Bromo-4-(chloromethyl)thiophene | HCID 12874109 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 23042157 | HCID 23042157 | 113.5% |
Reaction Steps
7.44 g of 4-phenoxyphenol and 5.52 g of potassium carbonate are stirred in 50 ml of anhydrous dimethylformamide for 1 hour at 70° C. 5.52 g of 2-bromo-4-chloromethylthiophene is then dripped in, and the mixture is stirred for a further 12 hours at 80° C., and at room temperature (approx. 20° C.) overnight. The mixture is then stirred into 500 ml of ethyl acetate and washed three times with water. After drying over sodium sulfate and removal of the solvent, the residue is recrystallized from n-hexane. There is obtained 10.7 g of 2-bromo-4-[(phenoxyphenoxy)-methyl]-thiophene; colorless powder; m.p.: 90° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04943584 |
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| Source dataset | uspto-grants-1990_07 |
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| ORD ID | ord-ec1b8f9b6ccb498997b34037395a1d9a |
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| Source note | uspto-grants-1990_07 |
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