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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 233283생성일: 2026년 10월 23일

Hydrogen Bromide → 2-Bromo-3-[2-[2-(5-methyl-2-phenyl-4-oxazolyl)ethoxy]-5-pyridyl]propionitrile

https://huagongshe.com/ko/reaction/233283

반응식

참여 물질

역할이름HCID투입량
반응물Hydrogen BromideHCID 260—
반응물AcrylonitrileHCID 7855—
반응물5-Amino-2-[2-(5-methyl-2-phenyl-4-oxazolyl)ethoxy]pyridineHCID 11087722—
반응물Sodium NitriteHCID 23668193—
촉매HCID 178419072HCID 178419072—
용매AcetoneHCID 180—
용매WaterHCID 962—
생성물2-Bromo-3-[2-[2-(5-methyl-2-phenyl-4-oxazolyl)ethoxy]-5-pyridyl]propionitrileHCID 1093852748%

반응 조건

온도10 °C

반응 단계

To a mixture of 5-amino-2-[2-(5-methyl-2-phenyl-4-oxazolyl)ethoxy]pyridine (9.1 g), an aqueous solution of HBr (47%, 14.2 ml) and acetone (150 ml) was added dropwise, at temperature not exceeding 10° C. a solution of sodium nitrite (NaNO2) (2.33 g) in water (10 ml). The mixture was stirred for 30 minutes at 10° C., to which was added acrylonitrile (CH2 =CHCN) (12.1 ml). To the mixture was added, while stirring vigorously, copper(I) oxide (Cu2O) (0.1 g). The reaction mixture was stirred for further one hour at temperature ranging from 30° to 35° C., followed by concentration under reduced pressure. The concentrate was poured into water, which was made alkaline with a conc. ammonia water, followed by extraction with ethyl acetate. The ethyl acetate layer was washed with water and dried (MgSO4), then the solvent was distilled off under reduced pressure. The residual oily product was subjected to a silica gel column chromatography. From the fractions eluted with ethyl acetate--hexane (1:1, v/v), was obtained 2-bromo-3-[2-[2-(5-methyl-2-phenyl-4-oxazolyl)ethoxy]-5-pyridyl]propionitrile (6.11 g, 48%), which was recrystallized from ethyl acetate--hexane to give colorless crystals, m.p.93°-94° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05591862
출처 데이터셋uspto-grants-1997_01
ORD IDord-e61f7be9d7924046bc7d0b79ad900d0d
출처 메모uspto-grants-1997_01