HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1696731Erstellt: 25. Oktober 2026
2-Bromo-3-methylthiophene → 2-(2-Methoxy-ethyl)-3-methyl-thiophene
https://huagongshe.com/reaction/1696731
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 | — |
Reaktionsschritte
A part of a solution containing 2-bromo-3-methylthiophene CAS 14282-76-9 (1.5 g, 8.5 mmol) in dry diethyl ether was added drop-wise to a suspension of magnesium (308 mg, 12.7 mmol, 1.5 equiv.) in dry diethyl ether,until 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 temp., then the mixture was refluxed for two hours. After cooling down to room temp., the mixture was quenched with ammonium chloride solution saturated and extracted with tert. butylmethyl ether. The combined organic extracts were washed with water and brine, dried over magnesiumsulfate-dihydrate and purified on silica gel with eluent n-heptane and tert.butylmethyl ether. The title compound was obtained as light yellow oil: 490 mg, GC-MS (EI) M=156.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08163778B2 |
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| Quelldatensatz | uspto-grants-2012_04 |
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| ORD ID | ord-f836c39c55474ca4ad93cb9e0fc54551 |
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| Quellennotiz | uspto-grants-2012_04 |
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