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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 81533Erstellt: 24. Oktober 2026

Ethyl difluoroacetate → 1-(3-Bromophenyl)-2,2-difluoroethanone

https://huagongshe.com/de/reaction/81533

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl difluoroacetateHCID 9961—
EduktBenzene, 1-bromo-3-iodo-HCID 11561—
EduktButyllithiumHCID 178418339—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt1-(3-Bromophenyl)-2,2-difluoroethanoneHCID 86650253—

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

1-Bromo-3-iodo-benzene (22.5 g, 90 mmol, Aldrich) was dissolved in THF and cooled to −78° C. nBuLi (69.8 ml, 90 mmol) was added over 15 minutes and the reaction was stirred for 30 min. at −78° C. Difluoro-acetic acid ethyl ester (16.59 ml, 153 mmol, Aldrich) was added dropwise and stirring was continued for 3 hrs. After completion the reaction was quenched by the addition of 329 ml 2 M HCl solution and reaction was warmed to r.t. The phases were separated and the aqueous phases was extracted with Et2O. The organic phases were washed with water and brine, dried over Na2SO4 and concentrated under reduced pressure. The residue was purified by automated column chromatography (cyclohexane/ethyl acetate) to yield the title compound as a yellow oil. 1H-NMR (360 MHz, DMSO-d6): 8.18 (s, 1H), 8.02 (m, 2H), 7.61 (t, 1H), 7.21 (t, 1H, CHF2); GC/MS: 234 [(M+H)+].

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08846658B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-3718d39fb24641369c8a93360d8e97eb
Quellennotizuspto-grants-2014_09