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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1866849Erstellt: 24. Oktober 2026

Hydrochloric Acid → 4-Formyl-3,5-dimethylbenzoic acid

https://huagongshe.com/de/reaction/1866849

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktDimethylformamideHCID 6228—
Edukt4-Bromo-3,5-dimethylbenzoic acidHCID 17937142—
EduktButyllithiumHCID 178418339—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt4-Formyl-3,5-dimethylbenzoic acidHCID 57978864—

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

A solution of 4-bromo-3,5-dimethylbenzoic acid (0.92 g, 4 mmol) in THF (10 mL) was cooled down to −100° C. with N2(I)-Et2O bath and added n-butyllithium (1.6 M in hexanes, 5 mL, 8 mmol) slowly. After completion of addition, the reaction mixture was warmed to −78° C. and DMF (0.74 mL, 8 mmol) was added dropwise. The resulting mixture was stirred at −78° C. for 1.5 h and allowed to warm to −20° C., followed by the addition of 2N aqueous HCl (30 mL). The organic phase was separated and the aqueous phase was extracted with EtOAc, the combined organic phases were dried over MgSO4. The solvent was removed and the resulting residue was purified by flash column chromatography (eluent: EtOAc-hexanes-1:1) to yield 4-formyl-3,5-dimethyl-benzoic acid (10c).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07629488B2
Quelldatensatzuspto-grants-2009_12
ORD IDord-a44fef9a98e04f79b395aa9be1364564
Quellennotizuspto-grants-2009_12