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HRID 591046作成日:2026年10月27日

Diethyl Ether → 1-(2-Hydroxy-6-methylphenyl)ethanone

https://huagongshe.com/reaction/591046

反応式

関与物質

役割名称HCID仕込み量
反応物Diethyl EtherHCID 3283—
反応物TriethylamineHCID 8471—
反応物Ammonium ChlorideHCID 25517—
反応物Ethyl 2-hydroxy-6-methylbenzoateHCID 584222—
反応物HCID 178418573HCID 178418573—
溶媒TolueneHCID 1140—
生成物1-(2-Hydroxy-6-methylphenyl)ethanoneHCID 1115940172.1%

反応手順

A solution of methyl magnesium bromide 3M in diethyl ether (18.5 mL, 55.5 mmol) and triethylamine (6.0 mL, 44.4 mmol) in anhydrous toluene (14 mL) was cooled to 0° C. 6-methylsalicylic acid ethyl ester (2.0 g, 11.1 mmol) in anhydrous toluene (14 mL) was added dropwise and the reaction mixture was stirred at room temperature for 16 hours. A saturated solution of ammonium chloride (10 mL) was added and the mixture was filtered over Celite®. The filtrate was diluted with ethyl acetate (20 mL) and water (10 mL) and layers were separated. The organic layer was washed with brine (10 mL), dried over sodium sulfate and evaporated to dryness. The residue was purified by flash chromatography on silica gel (cyclohexane/ethyl acetate: 9/1) to provide the desired ketone (26a) (1.21 g, 8.0 mmol, 72%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09238026B2
出典データセットuspto-grants-2016_01
ORD IDord-b494766faafc49a280d668843bc62aec
出典メモuspto-grants-2016_01