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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1004776Erstellt: 25. Oktober 2026

6-Bromo-1-hexanol → N-ethyl-N-(6-hydroxyhexyl)-4-bromoaniline

https://huagongshe.com/reaction/1004776

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt6-Bromo-1-hexanolHCID 77970—
EduktDiisopropylethylamineHCID 81531—
Edukt4-bromo-N-ethylanilineHCID 11745656—
LösungsmittelWaterHCID 962—
ProduktN-ethyl-N-(6-hydroxyhexyl)-4-bromoanilineHCID 18793525100%

Reaktionsbedingungen

Temperatur110 °C

Reaktionsschritte

36.8 g (184.1 mmols) of N-ethyl-4-bromoaniline, 48.1 ml (1.5-fold equivalent weight) of N,N-diisopropylethylamine and 28.9 ml (1.2 equivalent) of 6-bromohexanol were mixed, and the mixture obtained was heated at 110° C. for 14 hours in an atmosphere of argon. Water was added to the reaction solution obtained, which was then extracted with ethyl acetate. The organic layer obtained was dried with anhydrous magnesium sulfate and then concentrated. The residue thus obtained was heated under reduced pressure (160° C./0.3 torr), and the components distilled out were removed to obtain 55.6 g of crude N-ethyl-N-(6-hydroxyhexyl)-4-bromoaniline (yield: 100%; a dark-brown oily liquid).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06051722
Quelldatensatzuspto-grants-2000_04
ORD IDord-43f38d4b835a4852888afb02c2db9b16
Quellennotizuspto-grants-2000_04