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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 227620생성일: 2026년 10월 25일

4-Nitrobenzoyl chloride → 4-{[Tert-butyl(dimethyl)silyl]oxy}-1-(4-nitrophenyl)butan-1-one

https://huagongshe.com/reaction/227620

반응식

참여 물질

역할이름HCID투입량
반응물4-Nitrobenzoyl chlorideHCID 8502—
반응물Tert-butyl-(3-iodopropoxy)-dimethylsilaneHCID 11022956—
촉매HCID 178418397HCID 178418397—
용매BenzeneHCID 241—
용매DimethylformamideHCID 6228—
생성물4-{[Tert-butyl(dimethyl)silyl]oxy}-1-(4-nitrophenyl)butan-1-oneHCID 1160224647.5%

반응 단계

A mixture of Zn—Cu couple (2.68 g, 41.3 mmol) and tert-butyl(3-iodopropoxy)dimethylsilane (8.26 g, 27.5 mmol) in benzene (55 mL) and DMF (3.6 mL) was stirred vigorously at room temperature for 1 hour, heated to 60° C. for 4 hours, cooled to room temperature, and treated with a solution of 4-nitrobenzoyl chloride (3.4 g, 18.3 mmol) and (Ph3P)4Pd (0.847 g, 0.73 mmol) in benzene (36 mL) by cannula. The mixture was stirred for 1 hour, filtered through diatomaceous earth (Celite™), and partitioned between saturated NH4Cl and ethyl acetate. The aqueous phase was extracted three times with ethyl acetate and the combined extracts were washed with water and brine, dried (Na2SO4), filtered, and concentrated. The concentrate was purified by flash column chromatography on silica gel with 5% ethyl acetate/hexanes to provide 2.81 g of the desired product. MS(ESI(−)) m/e 322 (M−H)−.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07560552B2
출처 데이터셋uspto-grants-2009_07
ORD IDord-398a5d3424134113a4bd29f8ff47bc12
출처 메모uspto-grants-2009_07