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HRID 50012作成日:2026年10月26日

Phenol → 1-Chloro-2-(3-methyl-2-butenyloxy)-4-nitrobenzene

https://huagongshe.com/reaction/50012

反応式

関与物質

役割名称HCID仕込み量
反応物PhenolHCID 996—
反応物Potassium CarbonateHCID 11430—
反応物2-Chloro-5-nitrophenolHCID 69264—
反応物2-Butene, 1-bromo-3-methyl-HCID 70092—
触媒Tetrabutylammonium BromideHCID 74236—
溶媒Methyl Ethyl KetoneHCID 6569—
生成物1-Chloro-2-(3-methyl-2-butenyloxy)-4-nitrobenzeneHCID 12985690—

反応手順

A reaction mixture of 2-chloro-5-nitrophenol (50.6 g), anhydrous potassium carbonate (44.5 g), tetrabutylammonium bromide (4.7 g) and 4-bromo-2-methyl-2-butene (53.3 g, 90%) in methyl ethyl ketone (263 mL) was stirred at ambient temperature overnight. TLC of the reaction mixture showed traces of phenol remaining. Additional prenyl bromide (1 mL) was then added to the reaction mixture and stirred for 2 hours. The solvent was then removed from the reaction mixture. The residue of the reaction mixture was then treated with water and extracted into diethyl ether. The extract was washed with 2N sodium hydroxide and water, dried (MgSO4), filtered, and evaporated, to leave a brown solid which was recrystallised from ethyl acetate/isopropyl alcohol to give 1-chloro-2-(3-methyl-2-butenyloxy)-4-nitrobenzene, 49.5 g, a beige solid, a single spot on TLC (ethyl acetate:hexane, 20:80).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06710077B1
出典データセットuspto-grants-2004_03
ORD IDord-838b54af43ff4a799efbc77e83ff702c
出典メモuspto-grants-2004_03