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HRID 1373766作成日:2026年10月27日

Allyl bromide → 2-(Allyloxy)-1-bromo-5-methyl-3-nitrobenzene

https://huagongshe.com/reaction/1373766

反応式

関与物質

役割名称HCID仕込み量
反応物Allyl bromideHCID 7841—
反応物Potassium CarbonateHCID 11430—
反応物2-Bromo-4-methyl-6-nitrophenolHCID 29918—
溶媒AcetoneHCID 180—
生成物2-(Allyloxy)-1-bromo-5-methyl-3-nitrobenzeneHCID 1497744494.2%

反応手順

To a mixture of 2-bromo-4-methyl-6-nitrophenol (7.00 g, 30.2 mmol), K2CO3 (6.26 g, 45.3 mmol) in acetone (105 mL) was added allyl bromide (3.80 ml, 45.3 mmol). The reaction mixture was stirred at room temperature overnight. It was then heated at 40° C. for 5 hrs. Inorganic salts were filtered and washed with acetone. The filtrate was concentrated to give 7.74 g (94%) of the desired product. MS (DCI/NH3) m/z: 289.0 (M+NH4)+; 1H NMR (300 MHz, CD3OD) δ ppm 2.37 (s, 3 H) 4.61 (d, J=6.10 Hz, 2 H) 5.26 (dd, J=10.51, 1.80 Hz, 1 H) 5.39 (dd, J=17.29, 1.80 Hz, 1 H) 6.09 (m, 1 H) 7.63 (s, 1 H) 7.74 (s, 1 H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07163939B2
出典データセットuspto-grants-2007_01
ORD IDord-45249ef8d80d45258c2767c58c8dce87
出典メモuspto-grants-2007_01