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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 11900Erstellt: 24. Oktober 2026

2-(4-Amino-3-chloro-5-trifluoromethylphenyl)-2-tert-butylaminoethanol → 2-(4-Amino-3-chloro-5-trifluoromethyl-phenyl)-2-tert-butylaminoethanol hydrochloride

https://huagongshe.com/de/reaction/11900

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-(4-Amino-3-chloro-5-trifluoromethylphenyl)-2-tert-butylaminoethanolHCID 9997789—
LösungsmittelEthanolHCID 702—
LösungsmittelDiethyl EtherHCID 3283—
Produkt2-(4-Amino-3-chloro-5-trifluoromethyl-phenyl)-2-tert-butylaminoethanol hydrochlorideHCID 999778880%

Reaktionsschritte

1.0 g of 2-(4-amino-3-chloro-5-trifluoromethylphenyl)-2-tert-butylaminoethanol was dissolved in 20 ml of diethyl ether and filtered. Saturated solution of hydrogen chloride in isopropanol was added dropwise and acidified to pH=2. The precipitate was collected by filtration, washed with anhydrous ether, and dried to give crude 2-(4-amino-3-chloro-5-trifluoromethyl-phenyl)-2-tert-butylaminoethanol hydrochloride. The crude product was dissolved in absolute ethanol at a ratio of 1:5 w/v. Filtered, anhydrous ether was added dropwise until small amount of crystals was precipitated. Lyophilized and filtered to give 2-(4-amino-3-chloro-5-trifluoromethyl-phenyl)-2-tert-butylaminoethanol hydrochloride. Yield 80–90%; melting point 205–206° C. (dec). 1H-NMR (DMSO-d6) δ:1.24 (9H, s), 3.77(2H, d), 4.42–4.44(1H, m), 7.72(1H, s), 7.87(1H, s).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07098364B2
Quelldatensatzuspto-grants-2006_08
ORD IDord-b0b6eaf0998a4f67af847dbabab1ce48
Quellennotizuspto-grants-2006_08