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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 904879생성일: 2026년 10월 24일

Pyridine → Piperidine

https://huagongshe.com/ko/reaction/904879

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물AcetonitrileHCID 6342—
반응물NitromethaneHCID 6375—
반응물Benzenepropanenitrile, 4-amino-beta-oxo-HCID 96920—
용매IsopropanolHCID 3776—
생성물PiperidineHCID 8082—
생성물DabcoHCID 9237—
생성물1,1,3,3-TetramethylguanidineHCID 66460—

반응 단계

In accordance with the second procedure, the 4-alkanesulfonaminobenzoylacetonitrile is first prepared by reaction of an alkanesulfonylchloride with 4-amino-benzoylacetonitrile at room temperature in dry pyridine. This product is in turn reacted with a dialkylaminobenzaldehyde at reflux temperature in isopropyl alcohol, acetonitrile, nitromethane, or a similar polar solvent and in the presence of a catalytic amount of piperidine, or another catalyst of comparable basicity such as tetramethylguanidine or triethylenediamine, to yield the desired dye.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04420555
출처 데이터셋uspto-grants-1983_12
ORD IDord-f9c4427952c3423b91e2d1a258b32f99
출처 메모uspto-grants-1983_12