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HRID 1590416作成日:2026年10月27日

4-(1,1,4-Trimethylpentyl)phenylethyne → 4-(1,1,4-Trimethylpentyl)bromobenzene

https://huagongshe.com/reaction/1590416

反応式

関与物質

役割名称HCID仕込み量
反応物4-(1,1,4-Trimethylpentyl)phenylethyneHCID 14989668—
反応物TrimethylaluminumHCID 16682925—
反応物4-(1-Oxo-4-methyl-pentyl) bromobenzeneHCID 22409079—
溶媒HexaneHCID 8058—
生成物4-(1,1,4-Trimethylpentyl)bromobenzeneHCID 22409083—

反応手順

Reaction Scheme 6 discloses specific synthetic steps leading to 4-(1,1,4-trimethylpentyl)phenylethyne (Compound 34). In this synthetic route 4-(1-oxo-4-methyl-pentyl) bromobenzene (Compound 31, obtained for example as shown in Reaction Scheme 5) is reacted under a protective nitrogen atmosphere with trimethylaluminum in hexane to yield 4-(1,1,4-trimethyl-pentyl)bromobenzene (Compound 35). The bromobenzene derivative 35 is converted through the corresponding trimethylsilylethyne derivative 36 into the target intermediate 34 by treatment with trimethylsilyl ethyne and subsequently with KOH in isopropanol, as described above. ##STR10##

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05202471
出典データセットuspto-grants-1993_04
ORD IDord-dd1c397b01ec49dd9c16149a92b91ea6
出典メモuspto-grants-1993_04