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HRID 221213Erstellt: 23. Oktober 2026
6-Nitro-2H-1,4-benzoxazin-3(4H)-one → 6-amino-3,4-dihydro-2H-1,4-benzoxazin-3-one
https://huagongshe.com/de/reaction/221213
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 6-Nitro-2H-1,4-benzoxazin-3(4H)-one | HCID 2763683 | — |
| Edukt | Potassium borohydride | HCID 4192641 | — |
| Edukt | HCID 178418361 | HCID 178418361 | — |
| Katalysator | Cuprous chloride | HCID 62652 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Produkt | 6-amino-3,4-dihydro-2H-1,4-benzoxazin-3-one | HCID 2763681 | — |
Reaktionsschritte
To a suspension of 6-nitro-2H-1,4-benzoxazin-3(4H)-one 1 (0.5 g, 0.0026 mol) and CuCl (0.77 g, 0.0078 mol) in anhydrous methanol (25 mL), stirred at 25° C. was added potassium borohydride (0.98 g, 0.018 mol) in portions (exothermic with evolution of hydrogen gas). The reaction mixture was stirred at 25° C. for 30 min. The black precipitate formed was filtered and washed with methanol. The combined filtrate and washings was evaporated to give 6-amino-2H-benzo[b][1,4]oxazin-3(4H)-one which was purified by silica gel column chromatography using ethyl acetate. Brown solid (0.29 g, 67%). 1H NMR (400 MHz, CDCl3): δ 4.34 (s, 2H); 4.81 (s, 2H); 6.09 (dd, J=2.8, 8.4 Hz, 1H); 6.14 (d, J=2.8 Hz, 1H); 6.59 (d, J=8.4 Hz, 1H); 10.44 (s, 1H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08207163B2 |
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| Quelldatensatz | uspto-grants-2012_06 |
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| ORD ID | ord-2e98c9e1ed584d54ad37a534d8fce68c |
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| Quellennotiz | uspto-grants-2012_06 |
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