HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 397155Generated: October 26, 2026
Hydrochloric Acid → 6-Nitro-2-toluonitrile
https://huagongshe.com/reaction/397155
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 1,2-Dimethyl-3-nitrobenzene | HCID 6739 | — |
| Reactant | Butyl nitrite | HCID 10996 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 6-Nitro-2-toluonitrile | HCID 74669 | — |
Reaction Steps
A solution of 16 g (150 mmol) of n-butyl nitrite (97%) and 7.7 g (50 mmol) of 3-nitro-o-xylene (97%) in 50 ml of dimethylformamide is cooled to from −5 to −10° C., and a solution of 11 g (100 mmol) of potassium tert-butoxide in 50 ml of dimethylformamide is added at this temperature, over a period of 1.5 hours. The reaction mixture is stirred at room temperature for another 6 days. For work-up, the mixture is poured onto ice-water and adjusted to pH 1 using hydrochloric acid, and the aqueous phase is extracted with ethyl acetate. The organic phase is washed with water, dried over magnesium sulfate and concentrated. This gives 8.2 g of product. The 2-methyl-6-nitrobenzonitrile can be purified by silica gel chromatography using the mobile phase toluene. M.p.: 101-103° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06608209B2 |
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| Source dataset | uspto-grants-2003_08 |
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| ORD ID | ord-c5a458fa710449e4a62f83bfa96e7511 |
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| Source note | uspto-grants-2003_08 |
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