Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | Stannous chloride dihydrate | HCID 61436 | — |
| Edukt | Methyl 4-amino-3-methylbenzoate | HCID 2736799 | — |
| Edukt | Sodium Nitrite | HCID 23668193 | — |
| Lösungsmittel | Hydrochloric Acid | HCID 313 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | Methyl 4-hydrazinyl-3-methylbenzoate | HCID 59255931 | — |
Reaktionsschritte
50 ml of conc. hydrochloric acid are added to methyl 4-amino-3-methylbenzoate (10 g, 61 mmol) and the mixture is cooled down to −15° C. A solution of sodium nitrite (6.3 g, 91 mmol) in 50 ml of water is added dropwise in such a way that the temperature does not exceed −5° C. After stirring at −10° C. for 4 h, a solution of tin(II) chloride dihydrate in 50 ml of conc. hydrochloric acid is added dropwise to the suspension, with the reaction temperature not exceeding −5° C. The viscous suspension is stirred at RT for 15 h before it is adjusted to pH 14 with 200 ml of sodium hydroxide solution (10 N). The reaction mixture is filtered through kieselguhr and Extrelut® (60 g) and rinsed with 2 l of chloroform. The organic phase which is obtained is washed with water (2×200 ml), dried over sodium sulphate and evaporated in vacuo. The residue is stirred up with 120 ml of petroleum ether and filtered. Yield: 6.3 g
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08207349B2 |
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| Quelldatensatz | uspto-grants-2012_06 |
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| ORD ID | ord-2187742b18c349f082375daad76c1765 |
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| Quellennotiz | uspto-grants-2012_06 |
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