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HRID 710220作成日:2026年10月26日

Toluene → 2-Cyclopropyl 5-nitrobenzenamine

https://huagongshe.com/reaction/710220

反応式

関与物質

役割名称HCID仕込み量
反応物TolueneHCID 1140—
反応物Cesium carbonateHCID 10796—
反応物2-Bromo-5-nitroanilineHCID 82607—
反応物2-Cyclopropyl-6-methyl-1,3,6,2-dioxazaborocane-4,8-dioneHCID 44138342—
触媒palladium(II) acetateHCID 167845—
溶媒WaterHCID 962—
生成物2-Cyclopropyl 5-nitrobenzenamineHCID 5806580170%

反応手順

In a 250 mL round bottom flask to a solution of 2-bromo 5-nitroaniline (2.30 g, 10.60 mmol) in toluene (90 mL) tricyclohexylphosphine (0.89 g, 3.18 mmol), Cs2CO3 (17.22 g, 52.99 mmol), cyclopropylboronic acid MIDA ester (2.92 g, 14.84 mmol) and 10 ml de-ionized water were added and the solution was degassed with nitrogen for 30 minutes. To the above solution Pd(OAc)2 (0.36 g, 1.59 mmol) was added under nitrogen and the reaction mixture was refluxed for 12 hours. LC MS analysis of the crude reaction indicated the completion of the reaction. The crude reaction mixture was filtered on Celite pad and the volatiles were removed under reduced pressure. The dark brown oil was worked-up with 2×100 mL ethyl acetate and water (100 mL), dried on MgSO4 and ethyl acetate was evaporated under reduced pressure. The crude reaction mixture was separated by column chromatography to give 2-cyclopropyl-5-nitrobenzeneamine in 70% yield.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09181222B2
出典データセットuspto-grants-2015_11
ORD IDord-32711bfdb24d457ea9bcd8fb8af08a8f
出典メモuspto-grants-2015_11