Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Tetrahydrofuran | HCID 8028 | — |
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | 6-amino-3,4-dihydro-2H-1,4-benzoxazin-3-one | HCID 2763681 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | 3,4-Dihydro-2H-1,4-benzoxazin-6-amine | HCID 11344102 | 51% |
Reaktionsschritte
6-Amino-2H-benzo[b][1,4]oxazin-3(4H)-one (590 mg, 3.6 mmol) was added to THF solution of borane tetrahydrofuran complex (9 mL, 1M solution) and the reaction mixture was refluxed for 2.5 h. EtOH (2 mL) was added and stirred at 70° C. for 1 h before 1 mL HCl (conc.) was added. The mixture was stirred at 80° C. overnight then the volatiles were removed under vacuum to leave a crude reside. The residue was dissolved in water, NaOH was added until pH˜10, and the mixture was extracted with CH2Cl2. The organic phase was washed with water and the solvent was removed under vacuum. The residue was purified by column chromatography on silica gel to give the product (274 mg, 51%) as a colorless oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07312233B2 |
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| Quelldatensatz | uspto-grants-2007_12 |
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| ORD ID | ord-1601d7a75e584161bfbcc0680fb928ec |
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| Quellennotiz | uspto-grants-2007_12 |
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