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HRID 329706作成日:2026年10月26日

Benzene, [1-[(trimethylsilyl)oxy]ethenyl]- → 2-Phenylacetophenone

https://huagongshe.com/reaction/329706

反応式

関与物質

役割名称HCID仕込み量
反応物Benzene, [1-[(trimethylsilyl)oxy]ethenyl]-HCID 117406—
反応物Benzenediazonium tetrafluoroborateHCID 5284485—
溶媒PyridineHCID 1049—
溶媒Diethyl EtherHCID 3283—
生成物2-PhenylacetophenoneHCID 994870.1%

反応条件

温度0 °C

反応手順

0.97 mmol of (1-phenylethenyl)oxytrimethylsilane was placed in a 20-ml flask, followed by the addition of 3 ml of pyridine as a solvent. 1.3 mmol of benzenediazonium tetrafluoroborate was added to the flask. The resulting mixture was stirred at 0° C. in a nitrogen atmosphere for 2 hours. The reaction mixture was diluted with diethyl ether and washed with 1.5 N hydrochloric acid, water and a saturated aqueous solution of common salt, successively. The organic phase was dried over magnesium sulfate and distilled under a reduced pressure to remove the solvent. The obtained oily mixture was subjected to silica gel thin-layer chromatography to obtain 0.68 mmol of benzyl phenyl ketone.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04892936
出典データセットuspto-grants-1990_01
ORD IDord-515947eac51f4236977fc35b3ddaaa6e
出典メモuspto-grants-1990_01