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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 471675Generated: October 25, 2026

Phosphate → 2-Formyl-6-nitrobenzonitrile

https://huagongshe.com/reaction/471675

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphateHCID 1061—
Reactant6-Nitro-2-toluonitrileHCID 74669—
ReactantDimethylformamide dimethyl acetalHCID 78373—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
Product2-Formyl-6-nitrobenzonitrileHCID 8665747419%

Reaction Conditions

Temperature130 °C

Reaction Steps

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 solvent 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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08633186B2
Source datasetuspto-grants-2014_01
ORD IDord-c9150c4a039244189cb633e284c34382
Source noteuspto-grants-2014_01