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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1614816생성일: 2026년 10월 26일

Hydrochloric Acid → 1-(3-Methoxyphenyl)-1-(2-methylphenyl)-1-propanol

https://huagongshe.com/reaction/1614816

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Ammonium ChlorideHCID 25517—
반응물3'-MethoxypropiophenoneHCID 584765—
반응물HCID 178424303HCID 178424303—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물1-(3-Methoxyphenyl)-1-(2-methylphenyl)-1-propanolHCID 21266291438.6%

반응 단계

To a solution of 2-methylphenyl magnesium bromide (prepared from 4.9 g magnesium turnings and 24 ml of 2-bromotoluene) in dry THF (300 ml) was added dropwise a solution of 3'-methoxypropiophenone (25.9 g, 0.16 mol) in dry THF (200 ml). When addition was complete the mixture was heated at reflux temperature for 2 h. Water (250 ml) was added followed by a saturated ammonium chloride solution (250 ml) and the mixture was left overnight. A 4 N hydrochloric acid solution was added until a clear solution was obtained and the phases was separated. The organic phase was dried over magnesium sulphate and the solvent evaporated in vacuo. The residue was submitted to flash chromatography on silica gel (690 g) using a gradient of n-heptane in ethyl acetate to give 28.2 g (55%) of 1-(3-methoxyphenyl)-1-(2-methylphenyl)-1-propanol. A mixture of 1-(3-methoxyphenyl)-1-(2-methylphenyl)-1-propanol (26.2 g, 0.10 mol), isopropanol (300 ml) and a 6 N solution of sulphuric acid (150 ml) was stirred at room temperature for 2 h. The reaction mixture was neutralised with a 4 N sodium hydroxide solution and extracted with ethyl acetate (2×200 ml). The combined organic phases was dried over magnesium sulphate and the solvent was evaporated in vacuo. The residue was submitted to flash chromatography on silica gel (800 g) using n-heptane as eluent to give 18.4 g (76%) of 1-(3-methoxyphenyl)-1-(2-methylphenyl)-1-propene.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05198451
출처 데이터셋uspto-grants-1993_03
ORD IDord-c53928a727ca4fc8bcc9618e9842793e
출처 메모uspto-grants-1993_03