Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Tert-Butyl nitrite | HCID 10906 | — |
| Edukt | 2-Methyl-6-nitroaniline | HCID 11298 | — |
| Edukt | Dimethyl Disulfide | HCID 12232 | — |
| Katalysator | Copper | HCID 23978 | — |
| Produkt | 2-Methyl-6-nitrothioanisole | HCID 18757272 | — |
Reaktionsschritte
226 g (1.97 mmol) of tert-butyl nitrite and 100 g of copper powder are initially charged in 300 ml of dimethyl disulfide, and a solution of 200 g (1.32 mol) of 2-methyl-6-nitroaniline in 700 ml of dimethyl disulfide is added dropwise at 50-55° C. The mixture is then stirred at 75° C. for 8 hours. For work-up, the solid is filtered off with suction and the solution is diluted with methylene chloride and extracted with dilute hydrochloric acid. The organic phase is washed with saturated aqueous NaHCO3 solution, dried over sodium sulfate, filtered off and concentrated using a rotary evaporator. Excess dimethyl disulfide is removed under oil pump vacuum. This gives 271 g (99%) of a dark-red oil, purity according to HPLC 87%.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06608209B2 |
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| Quelldatensatz | uspto-grants-2003_08 |
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| ORD ID | ord-40b4362529454619938db5cb473be91e |
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| Quellennotiz | uspto-grants-2003_08 |
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