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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 7001Erstellt: 24. Oktober 2026

Dimethylformamide → 3-Bromo-5-fluorobenzaldehyde

https://huagongshe.com/de/reaction/7001

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylformamideHCID 6228—
Edukt1,3-Dibromo-5-fluorobenzeneHCID 137003—
EduktButyllithiumHCID 178418339—
LösungsmittelDiethyl EtherHCID 3283—
Produkt3-Bromo-5-fluorobenzaldehydeHCID 21986246100%

Reaktionsschritte

To a solution of 3,5-dibromofluorobenzene in diethyl ether (100 cm3) at −78° C. was added n-butyl lithium (2.5 M, 8 cm3, 20 mmol) dropwise. After 30 min. the mixture was treated with DMF (20 cm3) in diethyl ether (10 cm3) and stirring was continued at −78° C. After 30 min. the mixture was quenched with dilute HCl aq., separated and the aqueous layer was extracted with EtOAc. The combined organic layers were combined, washed with water, brine, dried (MgSO4) and evaporated to give 3-fluoro-5-bromobenzaldehyde (4.0 g, 19.7 mmol, 100%) as an oil: 1H NMR (CDCl3) δ inter alia 7.50–7.53 (m, 2H), 7.82 (s, 1H) and 9.93 (m, 1H); MS (EI) m/z 202, 204 [M+].

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07084168B2
Quelldatensatzuspto-grants-2006_08
ORD IDord-9ecd93464dc648fe987299a1452499ec
Quellennotizuspto-grants-2006_08