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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-Bromo-3-methylthiopheneHCID 84314—
EduktEthanol, 2-methoxy-, 1-(4-methylbenzenesulfonate)HCID 86977—
EduktMagnesiumHCID 5462224—
LösungsmittelDiethyl EtherHCID 3283—
Produkt2-(2-Methoxy-ethyl)-3-methyl-thiopheneHCID 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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08163778B2
Quelldatensatzuspto-grants-2012_04
ORD IDord-f836c39c55474ca4ad93cb9e0fc54551
Quellennotizuspto-grants-2012_04