Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1060060Erstellt: 26. Oktober 2026

Water → 3-(4-Chloro-3-ethylphenoxy)aniline

https://huagongshe.com/reaction/1060060

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
Edukt3-(4-Chloro-3-ethylphenoxy)-1-nitrobenzeneHCID 11065754—
KatalysatorZincHCID 23994—
LösungsmittelAcetic AcidHCID 176—
Produkt3-(4-Chloro-3-ethylphenoxy)anilineHCID 11021230112,1%

Reaktionsschritte

EX-8B) To a solution of 3-(4-chloro-3-ethylphenoxy)-1-nitrobenzene (10 g, 0.036 mol) from EX-A in 400 mL of glacial acetic acid and 1 mL of water was added zinc metal (20 g, 0.305 mol) at room temperature, and the resultant mixture was stirred for 1 h. The reaction mixture was filtered through celite. The filtrate was neutralized with ammonium hydroxide and extracted with diethyl ether. The organic layer was washed with water and brine, dried over MgSO4, and concentrated in vacuo to give 10 g (100%) of the desired 3-(4-chloro-3-ethylphenoxy)aniline product as a dark orange oil, which was greater than 90% pure by reverse phase HPLC analysis. HRMS calcd. for C14H14ClNO: 248.0842 [M+H]+, found: 248.0833.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06521607B1
Quelldatensatzuspto-grants-2003_02
ORD IDord-f20a67beeb5347b0b2a98e1eefd2e43f
Quellennotizuspto-grants-2003_02