HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1009013Erstellt: 25. Oktober 2026
2-Bromo-3-methylthiophene → 2-(2-Methoxy-ethyl)-3-methyl-thiophene
https://huagongshe.com/reaction/1009013
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 2-Bromo-3-methylthiophene | HCID 84314 | — |
| Edukt | Ethanol, 2-methoxy-, 1-(4-methylbenzenesulfonate) | HCID 86977 | — |
| Edukt | Magnesium | HCID 5462224 | — |
| Lösungsmittel | Diethyl Ether | HCID 3283 | — |
| Produkt | 2-(2-Methoxy-ethyl)-3-methyl-thiophene | HCID 66857153 | 36,9% |
Reaktionsschritte
Some drops from a solution of 2-bromo-3-methylthiophene (1.5 g, 8.5 mmol) in dry diethyl ether was added to a suspension of magnesium (308 mg, 12.7 mmol, 1.5 equiv.) in dry diethyl ether until the Grignard reagent began to form and the mixture started to reflux. The remaining solution was added dropwise. A solution of toluene-4-sulfonic acid 2-methoxy-ethyl ester (2.9 g, 12.7 mmol, 1.5 equiv.) in dry diethyl ether was added dropwise at room temperature, and the mixture was refluxed for two hours. After cooling to room temperature, the mixture was quenched with saturated ammonium chloride solution and extracted with tert. butylmethyl ether. The combined organic extracts were washed with water, brine, dried over magnesiumsulfate-dihydrate, filtered and evaporated to give a yellow oil. After purification on silica gel, 490 mg of the title compound were obtained as a light yellow oil. GC-MS (EI): M=156
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07973051B2 |
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| Quelldatensatz | uspto-grants-2011_07 |
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| ORD ID | ord-265b441da79247a884bec2a35fd4a725 |
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| Quellennotiz | uspto-grants-2011_07 |
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