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HRID 225948作成日:2026年10月27日

Phenol → Phenoxymethyl ketone

https://huagongshe.com/reaction/225948

反応式

関与物質

役割名称HCID仕込み量
反応物PhenolHCID 996—
反応物1,3-Dibromo-2-propanoneHCID 69952—
反応物Potassium FluorideHCID 522689—
溶媒DimethylformamideHCID 6228—
生成物Phenoxymethyl ketoneHCID 1340809050%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07557133B2
出典データセットuspto-grants-2009_07
ORD IDord-8187fab915144f549df77aa45aa50258
出典メモuspto-grants-2009_07