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HRID 37832作成日:2026年10月25日

Benzyl Bromide → 2-(Benzyloxy)-1-chloro-4-nitrobenzene

https://huagongshe.com/reaction/37832

反応式

関与物質

役割名称HCID仕込み量
反応物Benzyl BromideHCID 7498—
反応物Potassium CarbonateHCID 11430—
反応物2-Chloro-5-nitrophenolHCID 69264—
溶媒AcetoneHCID 180—
生成物2-(Benzyloxy)-1-chloro-4-nitrobenzeneHCID 1288193399%

反応手順

Benzyl bromide (0.6 mL, 5.04 mmol) was added dropwise to a mixture of 2-chloro-5-nitro-phenol (800 mg, 4.61 mmol) and potassium carbonate (1.27 g, 9.22 mmol) in acetone (20 mL) at room temperature and heated at reflux for 2 h. Inorganic salts were filtered off and washed with acetone (20 mL). The combined filtrate and washings were concentrated in vacuo, the resulting residue then being dissolved in ethyl acetate (25 mL) and washed successively with water (2×20 mL), brine (20 mL), dried over anhydrous sodium sulfate and concentrated in vacuo to yield 2-benzyloxy-1-chloro-4-nitro-benzene (1.20 g, 99%) as a cream solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08524705B2
出典データセットuspto-grants-2013_09
ORD IDord-c6b6cd300ebe4d5bb2b195e5a8862289
出典メモuspto-grants-2013_09