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HRID 1009013作成日:2026年10月27日

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

https://huagongshe.com/reaction/1009013

反応式

関与物質

役割名称HCID仕込み量
反応物2-Bromo-3-methylthiopheneHCID 84314—
反応物Ethanol, 2-methoxy-, 1-(4-methylbenzenesulfonate)HCID 86977—
反応物MagnesiumHCID 5462224—
溶媒Diethyl EtherHCID 3283—
生成物2-(2-Methoxy-ethyl)-3-methyl-thiopheneHCID 6685715336.9%

反応手順

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

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07973051B2
出典データセットuspto-grants-2011_07
ORD IDord-265b441da79247a884bec2a35fd4a725
出典メモuspto-grants-2011_07