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HRID 50013作成日:2026年10月25日

Hexane → 4-Chloro-3-(3-methyl-2-butenyloxy)benzenamine

https://huagongshe.com/reaction/50013

反応式

関与物質

役割名称HCID仕込み量
反応物HexaneHCID 8058—
反応物Ethyl AcetateHCID 8857—
反応物1-Chloro-2-(3-methyl-2-butenyloxy)-4-nitrobenzeneHCID 12985690—
触媒IronHCID 23925—
溶媒Hydrochloric AcidHCID 313—
溶媒EthanolHCID 702—
溶媒WaterHCID 962—
溶媒Diethyl EtherHCID 3283—
生成物4-Chloro-3-(3-methyl-2-butenyloxy)benzenamineHCID 12985691—

反応手順

To a refluxing well-stirred suspension of iron powder (19.6 g, 100 mesh) in ethanol (60 mL), water (13.4 mL) and 36% hydrochloric acid (1.4 mL) was added 1-chloro-2-(3-methyl-2-butenyloxy)-4-nitrobenzene (24 g) in portions over 15-30 minutes. After 3 hours thin-layer chromatography (TLC) (ethyl acetate:hexane, 40:60) showed no substrate. The reaction mixture was then filtered hot and the iron oxide filter cake was washed with hot ethanol. The combined ethanol washes were evaporated to produce a residue. The residue was taken up in diethyl ether, washed with aqueous bicarbonate and water, dried (MgSO4), filtered, and evaporated, to give 4-chloro-3-(3-methyl-2-butenyloxy)benzenamine, 19.8 g of light brown oil.

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-c4e4019637dc499c97aa04611feb8ff6
出典メモuspto-grants-2004_03