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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 50013Erstellt: 24. Oktober 2026

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

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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHexaneHCID 8058—
EduktEthyl AcetateHCID 8857—
Edukt1-Chloro-2-(3-methyl-2-butenyloxy)-4-nitrobenzeneHCID 12985690—
KatalysatorIronHCID 23925—
LösungsmittelHydrochloric AcidHCID 313—
LösungsmittelEthanolHCID 702—
LösungsmittelWaterHCID 962—
LösungsmittelDiethyl EtherHCID 3283—
Produkt4-Chloro-3-(3-methyl-2-butenyloxy)benzenamineHCID 12985691—

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06710077B1
Quelldatensatzuspto-grants-2004_03
ORD IDord-c4e4019637dc499c97aa04611feb8ff6
Quellennotizuspto-grants-2004_03