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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 329706생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/329706

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참여 물질

역할이름HCID투입량
반응물Benzene, [1-[(trimethylsilyl)oxy]ethenyl]-HCID 117406—
반응물Benzenediazonium tetrafluoroborateHCID 5284485—
용매PyridineHCID 1049—
용매Diethyl EtherHCID 3283—
생성물2-PhenylacetophenoneHCID 994870.1%

반응 조건

온도0 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04892936
출처 데이터셋uspto-grants-1990_01
ORD IDord-515947eac51f4236977fc35b3ddaaa6e
출처 메모uspto-grants-1990_01