Ethyl trifluoroacetate → 1-(4-Chloro-2-fluorophenyl)-2,2,2-trifluoroethan-1-one

Temperatur

-78 °C

To a solution of n-BuLi (1.6 M in hexanes, 4.68 mmol, 2.93 mL) in dry THF was slowly added 4-chloro-2-fluoro-1-iodo-benzene 67h (3.9 mmol, 1.0 g) at −78° C. under N2. The mixture was stirred for 1 h at −78° C. and ethyl trifluoroacetate 67b (0.51 mL, 4.29 mmol) was added. The reaction was allowed to warm to room temperature overnight and was quenched with saturated aqueous NH4Cl solution. The mixture was extracted with EtOAc. The organic extracts were concentrated and purified by flash column chromatography (silica gel, 15% EtOAc/hexanes) to give compound 67i.

1. customat −78° C.
2. temperatureto warm to room temperature overnight
3. customwas quenched with saturated aqueous NH4Cl solution
4. extractionThe mixture was extracted with EtOAc
5. concentrationThe organic extracts were concentrated
6. custompurified by flash column chromatography (silica gel, 15% EtOAc/hexanes)

ORD-Eintrag

ord-faaa468eeef145c3bcf580b493226cdd

Quelldatensatz

uspto-grants-2014_05

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US08722658B2