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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1650336생성일: 2026년 10월 26일

Triethylamine → 5-Butylpyridine-2-carbonitrile

https://huagongshe.com/reaction/1650336

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물2-ChloroacrylonitrileHCID 70198—
반응물1-Dimethylamino-1-aza-3-n-butyl-1,3-butadieneHCID 86743901—
용매AcetonitrileHCID 6342—
생성물5-Butylpyridine-2-carbonitrileHCID 32937763%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04923993
출처 데이터셋uspto-grants-1990_05
ORD IDord-7db52327ff8b4b44938e3cd1c4358bb6
출처 메모uspto-grants-1990_05