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2-Methyl-3-butyn-2-ol → 2-{3-Methyl-3-hydroxybutynyl}-5-{2-(4-pyridyl)ethynyl}thiophene
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 2-Methyl-3-butyn-2-ol | HCID 8258 | — |
| 反応物 | 2-Bromo-5-{2-(4-pyridyl)ethynyl}thiophene | HCID 23358156 | — |
| 触媒 | Palladium | HCID 23938 | — |
| 生成物 | 2-{3-Methyl-3-hydroxybutynyl}-5-{2-(4-pyridyl)ethynyl}thiophene | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05594075 |
| 出典データセット | uspto-grants-1997_01 |
| ORD ID | ord-4959446866f7454595d5b68041b5c339 |
| 出典メモ | uspto-grants-1997_01 |