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HRID 482340作成日:2026年10月26日

Benzoyl chloride, 3-nitro- → Tert-butyl 3-nitrobenzoate

https://huagongshe.com/reaction/482340

反応式

関与物質

役割名称HCID仕込み量
反応物Benzoyl chloride, 3-nitro-HCID 8495—
反応物Potassium tert-butoxideHCID 23665647—
溶媒TetrahydrofuranHCID 8028—
生成物Tert-butyl 3-nitrobenzoateHCID 1196136963.5%

反応手順

Potassium t-butoxide (3.82 g, 32.30 mmol) is added to a solution of 3-nitrobenzoyl chloride (5.00 g, 26.94 mmol) in anhydrous THF (70 mL) and stirred under nitrogen for 2 hrs. The reaction mixture is concentrated in vacuo and partitioned between DCM and water. After separating the phases, the aqueous layer is back-extracted with ethyl acetate. The organic layers are combined, dried over anhydrous magnesium sulfate, filtered and then concentrated in vacuo. The crude product is purified on flash grade silica gel using 0-5% gradient of ethyl acetate in n-hexane. Fractions containing the product are combined, concentrated in vacuo, and then dried under high vacuum to provide the title compound as an oil (3.82 g, 17.1 mmol). 1H NMR (300 MHz, CDCl3) δ=1.63 (s, 9H); 7.62 (t, J=7.9 Hz, 1H); 8.29-8.41 (m, 2H); 8.78-8.80 (m, 1H). MS (Cl): [M+H]+ =224.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05795887
出典データセットuspto-grants-1998_08
ORD IDord-be1c5ba31c0b42b58399cd0d291adb63
出典メモuspto-grants-1998_08