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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 40279Erstellt: 25. Oktober 2026

Ammonia → 1-(4-Bromo-2-chlorophenyl)ethanamine

https://huagongshe.com/reaction/40279

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAmmoniaHCID 222—
EduktWaterHCID 962—
EduktSodium borohydrideHCID 4311764—
Edukt1-(4-Bromo-2-chlorophenyl)ethan-1-oneHCID 15560950—
KatalysatorTitanium isopropoxideHCID 11026—
LösungsmittelMethanolHCID 887—
Produkt1-(4-Bromo-2-chlorophenyl)ethanamineHCID 59843034—

Reaktionsbedingungen

Temperatur45 °C

Reaktionsschritte

A solution of 1-(4-bromo-2-chlorophenyl)ethanone (2.430 g, 10 mmol), ammonia, 2.0 m solution in methanol (26 ml, 52 mmol) and titanium (iv) isopropoxide (6 ml, 21 mmol) was stirred for 16 h in a sealed vessel. Reaction then added to a freshly made suspension of sodium borohydride powder, 98% (4 g, 104 mmol) in MeOH (20 mL). Exothermic reaction started at 9:45 am, then continued to stir with a 45° C. external heating bath for 45 min. Water (10 mL) then added to reaction and stirred for an additional 10 min. Resulting white solid removed via filtration through Celite, and filtrated reduced in volume under reduced pressure. This suspension then partioned between 9:1 CHCl3/IPA (30 mL) and 1M NaOH (10 mL). Aqueous further extracted with 9:1 CHCl3/IPA (2×10 mL). Combined organics dried over MgSO4, concentrated, then purified on silica (80 g) eluting with 0>5% 2M NH3 in MeOH/DCM. MS (ESI pos. ion) m/z: 234/236 (MH+). Calc'd exact mass for C8H9BrClN: 233/235. 1-(4-bromo-2-chlorophenyl)ethanamine isolated as a colorless oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08524900B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-1f234297fe724243b9d09be0fb420028
Quellennotizuspto-grants-2013_09