Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Nitric Acid | HCID 944 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Benzenamine, N,N,2,6-tetramethyl- | HCID 69853 | — |
| Reactant | HCID 20485257 | HCID 20485257 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Sulfuric Acid | HCID 1118 | — |
| Product | HCID 20485272 | HCID 20485272 | — |
Reaction Steps
40 ml of 2,6-dimethyl-N,N-dimethylaniline was dissolved in 88 ml of concentrated sulfuric acid at a temperature below 15° C., followed by dropwise addition of 35 ml of concentrated nitric acid by maintaining the temperature below 15° C. Thereafter, the mixture was reacted for one hour, poured into cold water and then neutralized with sodium carbonate, whereby 3-nitro-2,6-dimethyl-N,N-dimethylaniline was precipitated in the form of crystals. The produced nitro compound was reduced, diazotized and then pyrolyzed to obtain 3-hydroxy-2,6-dimethyl-N,N-dimethylaniline. This phenol compound was dissolved in an alkaline solution and treated with excess dimethyl sulfate at 40°-45° C. The resulting 3-methoxy-2,6-dimethyl-N,N-dimethylaniline was dissolved in hydrochloric acid and then admixed with double molar amount of zinc chloride to precipitate a double salt. It was recrystallized from dilute hydrochloric acid to obtain the salt of formula V. M.p.: 162°-165° C., amount of zinc: 11.8% (calculated: 11.4%); infrared absorption spectra: 3100 cm-1, 1450 cm-1, 1260 cm-1, 1070 cm-1, 820 cm-1, 1600 cm-1 ; NMR (chemical shift): 3.4 ppm, 3.9 ppm, 2.4 ppm, 2.5 ppm, 7.1 ppm, 7.2 ppm, 7.0 ppm, 7.3 ppm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04377630 |
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| Source dataset | uspto-grants-1983_03 |
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| ORD ID | ord-895f7064d7db4456b3ba19bdc145b5f0 |
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| Source note | uspto-grants-1983_03 |
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