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HRID 234043作成日:2026年10月27日

2-Methyl-3-butyn-2-ol → 2-{3-Methyl-3-hydroxybutynyl}-5-{2-(4-pyridyl)ethynyl}thiophene

https://huagongshe.com/reaction/234043

反応式

関与物質

役割名称HCID仕込み量
反応物2-Methyl-3-butyn-2-olHCID 8258—
反応物2-Bromo-5-{2-(4-pyridyl)ethynyl}thiopheneHCID 23358156—
触媒PalladiumHCID 23938—
生成物2-{3-Methyl-3-hydroxybutynyl}-5-{2-(4-pyridyl)ethynyl}thiopheneHCID 23358155—

反応手順

The 2-ethynyl-5-(4-pyridyl)ethynyl thiophene is synthesized by the reaction sequence shown below. In the first step, bromination of 1-(2-thienyl)-2-(4-pyridyl)ethene followed by base-catalyzed dehydrohalogenation gives 2-bromo-5-{2-(4-pyridyl)ethynyl}thiophene (I): ##STR5## In the second step, the palladium catalyzed addition of 2-methyl-3-butyn-2-ol to compound I gives 2-{3-methyl-3-hydroxybutynyl}-5-{2-(4-pyridyl)ethynyl}thiophene (II): ##STR6## The term "Ph" in the palladium catalyst formula means "phenyl". In the third step, removal of the protecting group using KOH in methanol gives the acetylene-terminated thermoset monomer 2-ethynyl-5-(4-pyridyl)ethynyl thiophene (III): ##STR7##

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05594075
出典データセットuspto-grants-1997_01
ORD IDord-4959446866f7454595d5b68041b5c339
出典メモuspto-grants-1997_01