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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 532358생성일: 2026년 10월 26일

Water → 2-Bromo-1-(4-methoxy-3-morpholin-4-yl-5-trifluoromethylphenyl)ethanone

https://huagongshe.com/reaction/532358

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Thiosulfate ionHCID 1084—
반응물Phenyltrimethylammonium bromide dibromideHCID 17977687—
반응물4-[5-(1,1-Dimethoxyethyl)-2-methoxy-3-trifluoromethylphenyl]morpholineHCID 58085699—
용매MethanolHCID 887—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물2-Bromo-1-(4-methoxy-3-morpholin-4-yl-5-trifluoromethylphenyl)ethanoneHCID 5808571264%

반응 조건

온도7 °C

반응 단계

4-[5-(1,1-Dimethoxyethyl)-2-methoxy-3-trifluoromethylphenyl]morpholine (O2.004; 460 mg) was dissolved in a mixture of methanol (1.4 ml) and THF (4 ml), the mixture was cooled to 7° C., and phenyltrimethylammonium tribromide (530 mg) was added in portions while stirring. After stirring at RT for 3 h, the mixture was left to stand overnight. Then aqueous thiosulfate solution (0.8 ml; w=5%) and water (4 ml) were added, and the mixture was admixed with EA and extracted three times with EA. The combined extracts were dried over magnesium sulfate, filtered and concentrated. The residue was dissolved in a mixture of acetonitrile (20 ml) and water (0.5 ml) and admixed with TFA (0.5 ml) while stirring. After stirring at RT for 5 h, the solvent was drawn off, and the residue was admixed with water, neutralized with saturated sodium hydrogencarbonate solution and extracted three times with ethyl acetate. The combined extracts were dried over magnesium, filtered and concentrated. The crude product was purified using silica gel with ethyl acetate/heptane as the eluent. 200 mg of the desired compound were obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08853206B2
출처 데이터셋uspto-grants-2014_10
ORD IDord-f0fa7ba286ce423fb2672ce966199cf3
출처 메모uspto-grants-2014_10