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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 49663Generated: October 26, 2026

Dimethylformamide → 2-Methyl-6-nitrobenzaldoxime

https://huagongshe.com/reaction/49663

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 with stirring and suspended. 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 subsequently added dropwise at −40° C. over a period of 7 hours (if the mixture is cooled appropriately, the duration of this addition can be reduced at will; an extension has hitherto not been examined; temperature variations between −35 and −45° C. can be tolerated). By HPLC, it is checked that the starting material has been converted completely. The reaction discharge is subsequently added with stirring to a mixture of 300 ml of water and 300 ml of glacial acetic acid, at from −5 to 0° C. The reaction mixture is then poured into 6 kg of ice-water and the solid is separated off by filtration (without any problems, the flow resistance has not yet been determined) and washed twice with 500 ml of water each time (caution: the crude product smells strongly). 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 (without any problems, the flow resistance has not yet been determined) and dried in a vacuum drying cabinet at 50° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06706886B2
Source datasetuspto-grants-2004_03
ORD IDord-ba20e344dac4485885d71f806c79d828
Source noteuspto-grants-2004_03