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HRID 1650336作成日:2026年10月27日

Triethylamine → 5-Butylpyridine-2-carbonitrile

https://huagongshe.com/reaction/1650336

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物2-ChloroacrylonitrileHCID 70198—
反応物1-Dimethylamino-1-aza-3-n-butyl-1,3-butadieneHCID 86743901—
溶媒AcetonitrileHCID 6342—
生成物5-Butylpyridine-2-carbonitrileHCID 32937763%

反応手順

0.1 mole of 1-dimethylamino-1-aza-3-n-butyl-1,3-butadiene, 0.1 mole of 2-chloroacrylonitrile and 0.2 mole of triethylamine are heated in 100 ml of acetonitrile for 20 hours to 60° C. The reaction mixture is concentrated by evaporation and the residue is dissolved in dioxane. The solution is filtered and gaseous HCl is introduced. The batch is stirred for 15 minutes at room temperature and then concentrated by evaporation. The residue is partitioned between CH2Cl2 and 1N NaHCO3. The organic phase is dried, concentrated by evaporation and distilled under a high vacuum, affording 10.0 g (63%) of a yellowish oil with a boiling point of 86°-87° C./3·10-1 mbar.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04923993
出典データセットuspto-grants-1990_05
ORD IDord-7db52327ff8b4b44938e3cd1c4358bb6
出典メモuspto-grants-1990_05