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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 46577생성일: 2026년 10월 24일

Pyridine → beta-(N-chloroacetyl-2,6-dimethylphenylamino)propionaldehyde

https://huagongshe.com/ko/reaction/46577

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참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물p-Toluenesulfonic acidHCID 6101—
반응물Chloroacetyl chlorideHCID 6577—
반응물Ethyl AcetateHCID 8857—
반응물Propane, 1,1-diethoxy-HCID 20858—
용매AcetoneHCID 180—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
생성물beta-(N-chloroacetyl-2,6-dimethylphenylamino)propionaldehydeHCID 20543839—

반응 조건

온도25 °C

반응 단계

An 8.6-g (0.076-mol) sample of chloroacetyl chloride was added dropwise to a solution of 16 g (0.06 mol) beta-2,6-dimethylphenylamino)propionaldehyde diethylacetal and 6 g (0.076 mol) pyridine in 60 ml ethyl acetate. A salt immediately precipitated. The reaction mixture was stirred at about 25° C. for about 18 hours. The reaction mixture was filtered and the filtrate was evaporated under reduced pressure to give an oil. The oil was mixed with 100 ml acetone, 25 ml water and about 0.5 g p-toluenesulfonic acid. The resulting solution was stirred for 2 hours at 25° C., diluted with water, and extracted with ethyl ether. The ether extracts were evaporated to give a pale yellow oil. The yellow oil was dissolved in dichloromethane, dried over magnesium sulfate, treated with silica, filtered and evaporated to give 12.3 g of an oil which partially crystallized to give the product. Infrared analysis showed amide carbonyl absorption at 6.0 micron and aldehyde carbonyl absorption at 5.8 micron. The product is tabulated in Table I as Compound No. 13-A.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04174210
출처 데이터셋uspto-grants-1979_11
ORD IDord-8e5ba7d470514b24a3b558424327f84c
출처 메모uspto-grants-1979_11