Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2425057Erstellt: 27. Oktober 2026

2-Bromo-3-methylthiophene → 2-(2-Methoxy-ethyl)-3-methyl-thiophene

https://huagongshe.com/reaction/2425057

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 CAS14282-76-9 (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
PatentnummerUS07964633B2
Quelldatensatzuspto-grants-2011_06
ORD IDord-94455c993f8841428b257b3430f0d43c
Quellennotizuspto-grants-2011_06