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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 420329Erstellt: 25. Oktober 2026

Hydrochloric Acid → 5-tert-Butyl-2-fluoro-benzaldehyde

https://huagongshe.com/reaction/420329

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktDimethylformamideHCID 6228—
EduktHexaneHCID 8058—
Edukt1-(1,1-Dimethylethyl)-4-fluorobenzeneHCID 136540—
EduktButyllithiumHCID 178418339—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt5-tert-Butyl-2-fluoro-benzaldehydeHCID 59409516—

Reaktionsbedingungen

Temperatur-45 °C

Reaktionsschritte

A solution of 1-tert-butyl-4-fluoro-benzene (4.54 g, 30 mmol) in THF (100 mL) cooled at −78° C. was treated dropwise with a 2.5M solution of nBuLi in hexane (24 mL, 59 mmol). The reaction mixture was stirred for 5 h at −45° C. then DMF (3.5 mL, 44 mmol) was added at −75° C. and the reaction mixture was stirred for 0.5 h at −75° C. The reaction mixture was poured onto 1N aq. HCl and extracted with Et2O. Combined organic layers were washed with brine, dried over Na2SO4, filtered and evaporated. The title compound was obtained after chromatographic purification (Combi Flash, 40 g silica gel, hexane to hexane-EtOAc 10:1) as a light yellow oil: TLC (hexane-EtOAc 10:1) Rf=0.48, HPLC RtA=2.10 min; 1H NMR (400 MHz, CDCl3): δ10.36 (s, 1H), 7.85 (dd, 1H), 7.62 (m, 1H), 7.08 (dd, 1H), 1.32 (s, 9H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08093406B2
Quelldatensatzuspto-grants-2012_01
ORD IDord-4272a5c506464c4e8293a5d378306f8b
Quellennotizuspto-grants-2012_01