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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 708804Erstellt: 25. Oktober 2026

Ethyl bromodifluoroacetate → Ethyl 2-(4-bromo-2,6-dimethylphenyl)-2,2-difluoroacetate

https://huagongshe.com/reaction/708804

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl bromodifluoroacetateHCID 69585—
Edukt5-Bromo-2-iodo-1,3-dimethylbenzeneHCID 2735573—
KatalysatorCopperHCID 23978—
LösungsmittelDimethyl SulfoxideHCID 679—
ProduktEthyl 2-(4-bromo-2,6-dimethylphenyl)-2,2-difluoroacetateHCID 11809867688,3%

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

To a degassed solution of 5-bromo-2-iodo-1,3-dimethylbenzene (3.9 g, 12.54 mmol) and ethyl 2-bromo-2,2-difluoroacetate (3.22 ml, 25.08 mmol) in DMSO (30 ml) was added copper (3.19 g, 50.2 mmol). The reaction mixture was stirred at 60° C. for 3 h, then cooled to r.t. and filtered. The filtrate was diluted with EtOAc and water, extracted with EtOAc (3×). The combined organic layer was washed with brine, dried with MgSO4, filtered and concentrated. The crude product was purified by flash chromatography to give Intermediate 7A (3.4 g, 11.07 mmol, 88% yield) as a colorless oil. 1H NMR (400 MHz, chloroform-d) δ ppm 1.32 (t, J=7.03 Hz, 3H) 2.44 (t, J=4.17 Hz, 6H) 4.32 (q, J=7.18 Hz, 2H) 7.23 (s, 2H). 19F NMR (376 MHz, chloroform-d) δ ppm −95.28 (br. s., 2F).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09174974B2
Quelldatensatzuspto-grants-2015_11
ORD IDord-43108a86b60045159095cf0762cf1d8c
Quellennotizuspto-grants-2015_11