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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 50013생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/50013

반응식

참여 물질

역할이름HCID투입량
반응물HexaneHCID 8058—
반응물Ethyl AcetateHCID 8857—
반응물1-Chloro-2-(3-methyl-2-butenyloxy)-4-nitrobenzeneHCID 12985690—
촉매IronHCID 23925—
용매Hydrochloric AcidHCID 313—
용매EthanolHCID 702—
용매WaterHCID 962—
용매Diethyl EtherHCID 3283—
생성물4-Chloro-3-(3-methyl-2-butenyloxy)benzenamineHCID 12985691—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06710077B1
출처 데이터셋uspto-grants-2004_03
ORD IDord-c4e4019637dc499c97aa04611feb8ff6
출처 메모uspto-grants-2004_03