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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2090339Erstellt: 26. Oktober 2026

Ammonia → 4-Bromo-alpha-methylbenzeneethanamine

https://huagongshe.com/reaction/2090339

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAmmoniaHCID 222—
Edukt1-(4-Bromophenyl)propan-2-oneHCID 736332—
EduktSodium borohydrideHCID 4311764—
KatalysatorTitanium isopropoxideHCID 11026—
LösungsmittelEthanolHCID 702—
Produkt4-Bromo-alpha-methylbenzeneethanamineHCID 205668—

Reaktionsschritte

To a mixture of 2.0 M of ammonia in ethanol (117 mL, 235 mmol, Aldrich, Cat. No. 392685) and titanium tetraisopropoxide (27.7 mL, 93.9 mmol, Aldrich, Cat. No. 377996) was added 1-(4-bromophenyl)acetone (10.0 g, 46.9 mmol, Alfa Aesar, Cat. No. A19028). The reaction mixture was stirred at r.t. under nitrogen overnight. Sodium tetrahydroborate (2.66 g, 70.4 mmol) was added. The mixture was stirred at r.t. for additional 3 h. The reaction mixture was quenched with 2M ammonia in water, and filtered. The solid was washed with AcOEt. The filtrate was concentrated to remove most ethanol, and then was washed with AcOEt twice. The combined organic layers were extracted with 1N HCl aqueous solution (twice). The aqueous HCl solutions were combined, and adjusted with ammonia aqueous solution to pH=10. The result solution was extracted with CH2Cl2. The organic layer was dried with MgSO4, filtered, and concentrated to afford the desired compound which was directly used in the next step reaction without further purification. LCMS (M+H)+: m/z=214.2.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08436008B2
Quelldatensatzuspto-grants-2013_05
ORD IDord-b1413a4f29a04d0095a49d9847b92f74
Quellennotizuspto-grants-2013_05