Reaktion #794854

Reaktionsgleichung

3-(3-Oxocyclobutyl)propanoic acid

3-(3-Oxo-cyclobutyl)-propionic acid

4-tert-butyl-2-nitroaniline

pyridine

T3P

→

12

Ausbeute 85.0%

N-(4-tert-Butyl-2-nitrophenyl)-3-(3-oxocyclobutyl)propanamide

Ausbeute 85.0%

Lösungsmittel

1,4-dioxane

EtOAc

Reaktionsbedingungen

Aufarbeitung

1. 1
   TemperaturThe reaction was cooled to r.t.
2. 2
   Waschenwashed with 2M NaOH (2×20 ml), 2M HCl (20 ml), brine (20 ml)
3. 3
   Trocknendried over MgSO4
4. 4
   Einengenconcentrated in vacuo
5. 5
   Sonstigeto give the crude product
6. 6
   SonstigeThe product was purified by silica flash column chromatography

Vorschrift

3-(3-Oxocyclobutyl)propanoic acid (10) (1.610 g, 11.3 mmol) and 4-tert-butyl-2-nitroaniline (11) (2.000 g, 10.3 mmol) were dissolved in 1,4-dioxane (20 ml) and pyridine (2.6 ml, 30.9 mmol) and T3P (50% solution in EtOAc) (9.1 ml, 15.5 mmol) was added at r.t. The reaction was heated to 100° C. and left for 7 hrs. The reaction was cooled to r.t., diluted with EtOAc (20 ml) and washed with 2M NaOH (2×20 ml), 2M HCl (20 ml), brine (20 ml), dried over MgSO4 and concentrated in vacuo to give the crude product. The product was purified by silica flash column chromatography using between 100% heptanes to 40% EtOAc:60% heptanes as eluent to give 12 as a yellow oil (2.776 g, 85%): MS (ESI+) for C17H22N2O4 m/z 319.25 [M+H]+, 341.00 [M+Na]+; LC purity 99% (UV) (ret. time, 2.11 min); 1H NMR (500 MHz, CDCl3) δ 10.28 (s, 1H), 8.66 (d, J=8.9 Hz, 1H), 8.20 (d, J=2.3 Hz, 1H), 7.70 (dd, J=8.9, 2.3 Hz, 1H), 3.30-3.12 (m, 2H), 2.86-2.69 (m, 2H), 2.50 (ddd, J=30.3, 14.9, 7.6 Hz, 3H), 2.07 (q, J=7.6 Hz, 2H), 1.34 (s, 9H).

Quelle