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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1677233생성일: 2026년 10월 26일

1,2-Dibromoethane → 2-[4,5-Dimethoxy-2-(1-methyl-2-phenyl-ethyl)-phenyl]-4,4-dimethyl-4,5-dihydro-oxazole

https://huagongshe.com/reaction/1677233

반응식

참여 물질

역할이름HCID투입량
반응물1,2-DibromoethaneHCID 7839—
반응물(2-Bromopropyl)benzeneHCID 102754—
반응물MagnesiumHCID 5462224—
반응물4,4-Dimethyl-2-(2,4,5-trimethoxy-phenyl)-4,5-dihydro-oxazole oxazolineHCID 67053420—
용매TetrahydrofuranHCID 8028—
용매Ethyl acetate hexaneHCID 21226206—
생성물2-[4,5-Dimethoxy-2-(1-methyl-2-phenyl-ethyl)-phenyl]-4,4-dimethyl-4,5-dihydro-oxazoleHCID 5959871060.9%

반응 조건

온도40 °C

반응 단계

To a rapidly stirring suspension of magnesium turnings (1.32 g, 54.5 mol) and in 35 mL tetrahydrofuran (THF) was added 1,2-dibromoethane (0.10 mL) in one portion. 2-bromo-1-phenylpropane (10.86 g, 54.5 mmol) was added at a rate that maintained the internal temperature at 40° C. After 2.5 hours the cloudy suspension was transferred via canula to a solution of 4,4-dimethyl-2-(2,4,5-trimethoxy-phenyl)-4,5-dihydro-oxazole oxazoline (10.013 g, 36.4 mmol) in 50 mL THF. After 18 hours the solution cooled to 0° C. and quenched by the slow addition of 10% NH4Cl. 500 mL H2O was added and the mixture was extracted with ethyl acetate, washed with H2O, and washed with brine. The combined organics were dried over Na2SO4, filtered and concentrated in vacuo to give a crude solid. Purifications via flash chromatography (4:1 hexane/ethyl acetate) afforded 2-[4,5-dimethoxy-2-(1-methyl-2-phenyl-ethyl)-phenyl]-4,4-dimethyl-4,5-dihydro-oxazole as a clear viscous oil (7.833 g, 41%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08008313B2
출처 데이터셋uspto-grants-2011_08
ORD IDord-1e3e5787331c46459022167b57af1e58
출처 메모uspto-grants-2011_08