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HRID 227620作成日:2026年10月25日

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

https://huagongshe.com/reaction/227620

反応式

関与物質

役割名称HCID仕込み量
反応物4-Nitrobenzoyl chlorideHCID 8502—
反応物Tert-butyl-(3-iodopropoxy)-dimethylsilaneHCID 11022956—
触媒HCID 178418397HCID 178418397—
溶媒BenzeneHCID 241—
溶媒DimethylformamideHCID 6228—
生成物4-{[Tert-butyl(dimethyl)silyl]oxy}-1-(4-nitrophenyl)butan-1-oneHCID 1160224647.5%

反応手順

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)−.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07560552B2
出典データセットuspto-grants-2009_07
ORD IDord-398a5d3424134113a4bd29f8ff47bc12
出典メモuspto-grants-2009_07