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HRID 405184Erstellt: 24. Oktober 2026

Hydrochloric Acid → 2-Bromo-4,6-bis(trifluoromethyl)benzaldehyde

https://huagongshe.com/de/reaction/405184

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktEthyl formateHCID 8025—
Edukt2,2,6,6-TetramethylpiperidineHCID 13035—
Edukt1-Bromo-3,5-bis(trifluoromethyl)benzeneHCID 67602—
EduktButyllithiumHCID 178418339—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt2-Bromo-4,6-bis(trifluoromethyl)benzaldehydeHCID 86674259—

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

A 2.59 M hexanes solution of n-BuLi (1.13 mL, 2.92 mmol) was added dropwise to a, 0° C., THF solution (4 mL) of 2,2,6,6-tetramethylpiperidine (0.50 mL, 2.92 mmol). After 5 min at 0° C., the solution was cooled to −78° C. and 1-bromo-3,5-bis(trifluoromethyl)benzene was added dropwise over 2 min. The resulting brown amber colored solution was stirred at −78° C. for an additional 20 min. Ethyl formate (0.587 mL, 7.30 mmol) was then added dropwise at −78° C. over 1 min. After 30 min at −78° C., 1 M aqueous HCl was added, the layers were separated and the organic layer was washed with 0.1 M aqueous HCl and 1 M aqueous. The organic layer was dried (Na2SO4), concentrated, and short path vacuum distilled to provide the title compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08748624B2
Quelldatensatzuspto-grants-2014_06
ORD IDord-9e6e1e238479481e94e033818886ccae
Quellennotizuspto-grants-2014_06