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HRID 1193484作成日:2026年10月27日

Benzyl Bromide → 1-Benzyloxy-3-methyl-2-nitrobenzene

https://huagongshe.com/reaction/1193484

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3-Methyl-2-nitrophenolHCID 21026—
溶媒DimethylformamideHCID 6228—
生成物1-Benzyloxy-3-methyl-2-nitrobenzeneHCID 334418788.3%

反応条件

温度90 °C

反応手順

A mixture of 3-methyl-2-nitrophenol (50 g, 0.326 mol), K2CO3 (45 g, 0.326 mol) and benzylbromide (61.4 g, 42.6 mL, 0.359 mol) in dry DMF (200 mL) was stirred at 90° C. for 3 hours under nitrogen. Most of the DMF was removed at reduced pressure and the residue was partitioned between water (300 mL) and ether (300 mL). The organic layer was washed with brine and dried (Na2SO4). Removal of the solvent provided (70 g, 88%) of 3-benzyloxy-2-nitrotoluene as an orange oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04810699
出典データセットuspto-grants-1989_03
ORD IDord-a704537da871413fb26b32dab55ba06d
出典メモuspto-grants-1989_03