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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 892501생성일: 2026년 10월 25일

Ammonium Chloride → 1-(2-Methoxyphenyl)-3-methyl-1-(2-pyridyl)-2-buten-1-ol

https://huagongshe.com/reaction/892501

반응식

참여 물질

역할이름HCID투입량
반응물Ammonium ChlorideHCID 25517—
반응물1-Bromo-2-methyl-1-propeneHCID 98560—
반응물2-(2-Methoxybenzoyl)pyridineHCID 603942—
반응물MagnesiumHCID 5462224—
용매TetrahydrofuranHCID 8028—
생성물1-(2-Methoxyphenyl)-3-methyl-1-(2-pyridyl)-2-buten-1-olHCID 1989559660.7%

반응 단계

43.84 g of 1-bromo-2-methylprop-1-ene in 150 ml of tetrahydrofuran were added dropwise to 9.8 g of magnesium in 50 ml of tetrahydrofuran while heating at reflux. After 1 hour the mixture was allowed to cool to room temperature, whereupon 47.7 g of 2-methoxyphenyl 2-pyridyl ketone in 200 ml of tetrahydrofuran were added slowly. After stirring for 2 hours at room temperature 200 ml of saturated ammonium chloride were added and the mixture was extracted with ethyl acetate. The organic extract was dried over sodium sulphate and evaporated. The residue was chromatographed on silica gel using ethyl acetate/petroleum ether (1:6) followed by ethyl acetate/petroleum ethyl (1:4) for the elution to yield 36.6 g of 1-(2-methoxyphenyl)-3-methyl-1-(2-pyridyl)-2-buten-1-ol in the form of an oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05118694
출처 데이터셋uspto-grants-1992_06
ORD IDord-59ac6b12727149d1a18c85ca6c5b4ed7
출처 메모uspto-grants-1992_06