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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 711813Erstellt: 23. Oktober 2026

Phosphate → 2-Formyl-6-nitrobenzonitrile

https://huagongshe.com/de/reaction/711813

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPhosphateHCID 1061—
Edukt6-Nitro-2-toluonitrileHCID 74669—
EduktDimethylformamide dimethyl acetalHCID 78373—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt2-Formyl-6-nitrobenzonitrileHCID 8665747419%

Reaktionsbedingungen

Temperatur130 °C

Reaktionsschritte

1,1-Dimethoxy-N,N-dimethylmethanamine (13.56 mL, 102 mmol) was added to a solution of 2-methyl-6-nitrobenzonitrile (15.0 g, 92.5 mmol) in anhydrous DMF (60 mL) under nitrogen and was heated at 130° C. for 15 h. Ice water (300 mL) was added, and the resultant dark precipitate was collected by filtration and dried under vacuum. Phosphate buffer (pH 7, 350 mL) and then NaIO4 (40 g, 187 mmol) were added to a solution of the dark precipitate in THF (350 mL) and stirred at rt for 3 h. The mixture was extracted with EtOAc, the combined extract was washed with brine and dried with MgSO4. The filtrate was concentrated and the residue was purified by chromatography on silica using the solven gradient hexanes→EtOAc, to give 3.07 g (19%) of the title compound as a yellow solid. 1H NMR (400 MHz, DMSO-d6) δ 8.15 (t, J=8.4 Hz, 1H), 8.41 (dd, J=1.2, 7.6 Hz, 1H), 8.62 (dd, J=1.2, 8.4 Hz, 1H), 10.25 (s, 1H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09181276B2
Quelldatensatzuspto-grants-2015_11
ORD IDord-0ae6a3f30d2c468ca4577605f5f0987c
Quellennotizuspto-grants-2015_11