Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Methanol | HCID 887 | — |
| Edukt | 1,2-Dibromoethane | HCID 7839 | — |
| Edukt | m-Fluorobenzenethiol | HCID 75710 | — |
| Edukt | Sodium methanolate methanol | HCID 23694274 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | 1-[(2-Bromoethyl)sulfanyl]-3-fluorobenzene | HCID 22470626 | — |
Reaktionsschritte
To 2 mL of a methanol solution containing 0.83 g of 28% sodium methoxide/methanol, 1.0 mL of 1,2-dibromoethane and 0.50 g of 3-fluorobenzenethiol were added under cooling with ice, the mixture was stirred at the same temperature for 1 hour, at room temperature for 2 hours, and at 50° C. for 1 hour, and then the reaction mixture was refluxed by heating for 5 hours. The reaction mixture was cooled to room temperature, and then ethyl acetate and water were added thereto. The organic layer was separated, washed with an aqueous saturated sodium chloride solution and dried over anhydrous magnesium sulfate, and the solvent was removed under reduced pressure. The residue thus obtained was purified by silica gel column chromatography [eluent; hexane] to obtain 0.62 g of a pale yellow oily substance, 1-(3-fluorophenyl)thio-2-bromoethane.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08524738B2 |
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| Quelldatensatz | uspto-grants-2013_09 |
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| ORD ID | ord-4c599ba040dc492a8ebc1ad9adb1f598 |
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| Quellennotiz | uspto-grants-2013_09 |
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