Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Edukt | Tert-butyl 4-methyl-3-nitrobenzoate | HCID 22451886 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Produkt | Tert-butyl 3-amino-4-methylbenzoate | HCID 13994424 | 102,8% |
Reaktionsschritte
The compound (29.3 g, 123 mmol) of step A was dissolved in methanol (500 ml), ferric chloride (FeCl3) (1.73 g, 10.7 mmol) and activated carbon (4.5 g) were added and the mixture was stirred at room temperature. Then, hydrazine monohydrate (20 ml, 412 mmol) was added, and the mixture was heated under reflux for 45 min. The reaction mixture was cooled, filtered through celite, and the solution was concentrated under reduced pressure. The obtained oil was diluted with an ethyl acetate-hexane=1:1 mixed solvent (300 ml), washed with saturated aqueous sodium hydrogen carbonate and saturated brine, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure to give the title compound (26.2 g) as a pale-yellow oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08513235B2 |
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| Quelldatensatz | uspto-grants-2013_08 |
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| ORD ID | ord-c57a976f843b46ec9ae2f67e497a12d9 |
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| Quellennotiz | uspto-grants-2013_08 |
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