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HRID 727179생성일: 2026년 10월 26일

Methanol → 1-(3-Chlorophenyl)ethanone

https://huagongshe.com/reaction/727179

반응식

참여 물질

역할이름HCID투입량
반응물MethanolHCID 887—
반응물Benzonitrile, m-chloro-HCID 13015—
반응물HCID 178418573HCID 178418573—
용매TetrahydrofuranHCID 8028—
생성물1-(3-Chlorophenyl)ethanoneHCID 14933—

반응 단계

Under a nitrogen atmosphere, 36.7 mL (0.11 mole) of methylmagnesium bromide (3.0M in diethyl ether) is stirred, and a solution of 13.8 grams (0.10 mole) of 3-chlorobenzonitrile in 50 mL of dry tetrahydrofuran is added slowly dropwise. Upon completion of addition, the reaction mixture is warmed to reflux where it is stirred for about 18 hours. After this time the reaction mixture is cooled to ambient temperature, and about 40 mL of methanol is added dropwise. Upon completion of addition, the reaction mixture is stirred for two hours and then filtered. The filtrate is then stirred for about 18 hours with 35 grams of silica gel and 100 mL of water. The mixture is filtered, and the filtrate is diluted with ethyl acetate. The mixture is then washed with water, and the organic layer is dried with magnesium sulfate. The mixture is filtered, and the filtrate is concentrated under reduced pressure, yielding methyl 3-chlorophenyl ketone.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05712281
출처 데이터셋uspto-grants-1998_01
ORD IDord-1518c00294774bacbe3ba301d4199895
출처 메모uspto-grants-1998_01