Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Acetic Acid | HCID 176 | — |
| Edukt | Dichloromethane | HCID 6344 | — |
| Edukt | Methyl 3-amino-5-morpholino-2-nitrobenzoate | HCID 58278827 | — |
| Katalysator | Iron | HCID 23925 | — |
| Produkt | HCID 178498372 | HCID 178498372 | 77% |
Reaktionsschritte
To a solution of methyl 3-amino-5-(4-morpholinyl)-2-nitrobenzoate (22 g) stirring at reflux in HOAc (400 mL) was added iron powder in portions (13 g). After the addition, the mixture was stirred at reflux for 5 h. It was cooled to room temperature and the solvent was removed in-vacuo. The residue was neutralized with aqueous Na2CO3 solution (1 L). It was extracted with EtOAc (500 mL×3). The combined organic layers were then concentrated in-vacuo and the residue was purified by silica gel chromatography eluted with MeOH:DCM=1:30 to afford the desired product as a solid (16.6 g, yield 77%). 1H NMR (300 MHz, CDCl3): δ ppm 2.67 (s, 3H), 3.17 (t, 4H, J=4.8 Hz), 3.90 (t, 4H, J=4.8 Hz), 3.98 (s, 3H), 7.44 (d, 1H, J=1.8 Hz), 7.54 (d, 1H, J=1.8 Hz); LC-MS: m/e=276 [M+1]+.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08541411B2 |
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| Quelldatensatz | uspto-grants-2013_09 |
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| ORD ID | ord-11df0b4a0a5748c59323ac6bebb39bcd |
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| Quellennotiz | uspto-grants-2013_09 |
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