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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 225948생성일: 2026년 10월 27일

Phenol → Phenoxymethyl ketone

https://huagongshe.com/reaction/225948

반응식

참여 물질

역할이름HCID투입량
반응물PhenolHCID 996—
반응물1,3-Dibromo-2-propanoneHCID 69952—
반응물Potassium FluorideHCID 522689—
용매DimethylformamideHCID 6228—
생성물Phenoxymethyl ketoneHCID 1340809050%

반응 단계

Thus obtained bromomethyl ketone derivative (X, 12.9 g, 31.0 mmol) and phenol (3.23 g, 1.2 Eq) were dissolved in dimethylformamide (30 ml), KF(4.53 g, 2.5 Eq) was added, and the mixture was stirred for two hours to give phenoxymethyl ketone derivative (XIb). This compound was dissolved in methanol (40 ml)-THF (100 ml) and was reacted by adding NaBH4 (2.35 g)-methanol solution (40 ml) (−10□-room temperature, two hours). The reaction was stopped by acetic acid, and the reaction mixture was distilled under reduced pressure to remove methanol. The residue was extracted with ethyl acetate (50 ml×2), washed with water and aqueous sodium chloride solution, dried (anhydrous Na2SO4), concentrated under reduced pressure, and separated-purified by column chromatography (ethyl acetate-hexane, 1:7) to give a compound (XIIb, 6.50 g, Yield 50%) in a diastereomeric form of which amino group is protected by benzyloxycarbonyl.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07557133B2
출처 데이터셋uspto-grants-2009_07
ORD IDord-8187fab915144f549df77aa45aa50258
출처 메모uspto-grants-2009_07