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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 627476Erstellt: 24. Oktober 2026

Water → 1-(2-Amino-5-bromophenyl)-2,2,2-trifluoroethanone

https://huagongshe.com/de/reaction/627476

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktSodium SulfateHCID 24436—
EduktSodium AzideHCID 33557—
Edukt1-(5-Bromo-2-fluorophenyl)-2,2,2-trifluoroethan-1-oneHCID 11369266—
LösungsmittelDimethyl SulfoxideHCID 679—
LösungsmittelEthyl AcetateHCID 8857—
Produkt1-(2-Amino-5-bromophenyl)-2,2,2-trifluoroethanoneHCID 46838802—

Reaktionsschritte

A solution of 1-(5-bromo-2-fluorophenyl)-2,2,2-trifluoroethanone (6.67 g, 24.6 mmol, Intermediate 8, step a) in DMSO (6.2 mL) was treated with NaN3 (1.76 g, 27.0 mmol) and stirred under air (lightly capped) at 95° C. for 1 hour. The brownish-red opaque reaction was then cooled to room temperature on an ice bath, diluted with EtOAc (49 mL), treated with SnCl2-dihydrate (6.66 g, 29.5 mmol) in several portions over ˜30 sec followed by water (1.33 mL, 73.8 mmol), and the mixture was stirred at room temperature for 30 min. The reddish solution with heavy off-white particulates was then treated with anhydrous Na2SO4 (˜6 g; ˜40 mmol; ˜400 mmol water capacity) and stirred vigorously for a few minutes. The mixture was then filtered over a bed of Celite®, and the cloudy orange filtrate was dry load flash chromatographed (˜60 g silica gel) with a heptane to 50% DCM/heptane gradient to provide the title compound as an orange oil that crystallized upon standing.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09309222B2
Quelldatensatzuspto-grants-2016_04
ORD IDord-2d8d3a4a5a534f8aa68e068d2ae1916b
Quellennotizuspto-grants-2016_04