Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Cyanamide | HCID 9864 | — |
| Edukt | N-bromobutanimide | HCID 67184 | — |
| Edukt | Sodium permanganate monohydrate | HCID 516876 | — |
| Edukt | Sodium Bisulfate | HCID 516919 | — |
| Edukt | Potassium tert-butoxide | HCID 23665647 | — |
| Edukt | 2-Methoxy-3-methylthio-4-(trifluoromethyl)benzoic acid | HCID 66957907 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Produkt | HCID 89766894 | HCID 89766894 | 26,9% |
Reaktionsschritte
3.71 g (33.1 mmol) of potassium tert-butoxide were added to a solution of 4.00 g (15.0 mmol) of 2-methoxy-3-(methylsulfanyl)-4-(trifluoromethyl)benzoic acid in 250 ml of methanol. The mixture was stirred for 10 minutes, and 1.07 g (25.5 mmol) of cyanamide and 4.81 g (27.0 mmol) of N-bromosuccinimide were then added in succession. The contents were then stirred at RT for 2 h. The mixture was then freed from the solvent on a rotary evaporator and the residue was taken up in a mixture of in each case 120 ml of acetonitrile and water. 7.21 g (45.1 mmol) of sodium permanganate monohydrate were added, and the mixture was stirred at RT for one week. During this week, both after one day and after a further day, in each case 3.6 g (22.5 mmol) of sodium permanganate monohydrate were added. For work-up, a 10% by weight strength solution of sodium bisulfate was added. On a rotary evaporator, at a temperature of at most 30° C., the solvent was substantially removed. The residue was cooled in an ice bath and then acidified with 1M hydrochloric acid. The mixture was extracted three times with ice-cold dichloromethane. The combined organic phases were freed from the solvent on a rotary evaporator and the residue was purified chromatographically, which gave 1.30 g of product of a purity of 80% by weight.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09167819B2 |
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| Quelldatensatz | uspto-grants-2015_10 |
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| ORD ID | ord-331770813eb748e7a0f3a5ada4bd4a81 |
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| Quellennotiz | uspto-grants-2015_10 |
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