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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 397149Generated: October 28, 2026

Dimethylformamide → 2-Methyl-6-nitrobenzaldoxime

https://huagongshe.com/reaction/397149

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
Reactant1,2-Dimethyl-3-nitrobenzeneHCID 6739—
ReactantButyl nitriteHCID 10996—
ReactantPotassium methoxideHCID 23664618—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
Product2-Methyl-6-nitrobenzaldoximeHCID 85361048—

Reaction Conditions

Temperature-40 °C

Reaction Steps

1200 ml of anhydrous DMF are initially charged in a 4 l reaction flask and cooled to −40° C. At this temperature, 336.5 g (4.56 mol) of potassium methoxide (95%) are added and suspended with stirring. A mixture of 300 g (1.92 mol) of 3-nitro-o-xylene (97%) and 274 g (2.52 mol) of n-butyl nitrite (95%) is then added dropwise at −40° C. over a period of 7 hours (if the mixture is cooled accordingly, the duration of this addition can be reduced as desired). The complete conversion of the starting material is checked by HPLC. The reaction discharge is then added with stirring, at from −5 to 0° C., to a mixture of 300 ml of water and 300 ml of glacial acetic acid. The reaction mixture is then poured onto 6 kg of ice-water and the solid is separated off by filtration and washed twice with in each case 500 ml of water. The crude product (HPLC: 96 area %) is purified by suspending the moist solid in 800 ml of toluene for 1.5 h. The solid is filtered off and dried at 50° C. in a vacuum drying cabinet.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06608209B2
Source datasetuspto-grants-2003_08
ORD IDord-40c365267c7c4d1ba3d2b0d0f1ca6f0e
Source noteuspto-grants-2003_08