HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Butyl nitrite → 3-(Dipropylcarbamoyl)benzoic acid
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Butyl nitrite | HCID 10996 | — |
| Edukt | N-Boc-cis-4-hydroxy-D-proline | HCID 688616 | — |
| Edukt | 3-Bromo-5-(methoxycarbonyl)benzoic acid | HCID 22593641 | — |
| Edukt | (4R)-1-Boc-4-(2-propen-1-yloxy)-D-proline | HCID 67315699 | — |
| Katalysator | Copper bromide (CuBr2) | HCID 24611 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Acetonitrile | HCID 6342 | — |
| Produkt | 3-(Dipropylcarbamoyl)benzoic acid | HCID 182769 | 97% |
Reaktionsschritte
Step G (2): 3-bromo-5-(methoxycarbonyl)benzoic acid. To a mixture of copper (II) bromide (5.5 g, 24.6 mmol), n-butyl nitrite (3.17 g, 30.75 mmol) and acetonitrile (300 mL) was added 3-amino-5-(methoxycarbonyl)benzoic acid (Step G (1), 4.0 g, 20.5 mmol) in aceonitrile (300 mL) over 30 min at 0° C. and the mixture was warmed up and stirred at rt for 3 h. H2O was added and acetonitrile was removed. Ethyl acetate (600 mL) was added and the mixture was washed with 3N HCl, H2O, dried over Na2SO4, and concentrated in vacuo to give the title compound (97% yield): 1H NMR (CDCl3, 500 MHz) δ ppm 3.96 (3H, s), 8.41 (1H, s), 8.41 (1H, s), 8.67 (1H, m). MS (ESI) (M−H)− 259.02.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US07745470B2 |
| Quelldatensatz | uspto-grants-2010_06 |
| ORD ID | ord-f1e12c8ab4c14f8c9ebf66d37ccca20b |
| Quellennotiz | uspto-grants-2010_06 |