HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 397149Generated: October 28, 2026
Dimethylformamide → 2-Methyl-6-nitrobenzaldoxime
https://huagongshe.com/reaction/397149
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 1,2-Dimethyl-3-nitrobenzene | HCID 6739 | — |
| Reactant | Butyl nitrite | HCID 10996 | — |
| Reactant | Potassium methoxide | HCID 23664618 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Methyl-6-nitrobenzaldoxime | HCID 85361048 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06608209B2 |
|---|
| Source dataset | uspto-grants-2003_08 |
|---|
| ORD ID | ord-40c365267c7c4d1ba3d2b0d0f1ca6f0e |
|---|
| Source note | uspto-grants-2003_08 |
|---|