Reaktion #160862

ord-b8bc12b6e8904d4c98cd4a08ecec8f0b

Reaktionsgleichung

O=C(c1cc(Cl)c[nH]1)C(Cl)(Cl)Cl
2,2,2-trichloro-1-(4-chloro-1H-Pyrrol-2-yl)ethanone
[NH4+]
ammonium
NC(=O)c1cc(Cl)c[nH]1
above compound
Ausbeute 92.0%
NC(=O)c1cc(Cl)c[nH]1
4-chloro-1H-pyrrole-2-carboxamide
Ausbeute 92.0%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    EinengenThe reaction mixture was concentrated in vacuo

Vorschrift

A solution of 2,2,2-trichloro-1-(4-chloro-1H-Pyrrol-2-yl)ethanone (14.0 g, 56.7 mmol) in THF (100 mL) was bubbled with ammonium gas for 2 h at room temperature. TLC analysis indicated that there was complete conversion of starting material. The reaction mixture was concentrated in vacuo to yield 7.5 g of the above compound (51.88 mmol, yield 92%). 1H-NMR (Acetone-d6) δ 10.92 (br s, 1H), 7.21 (br s, 1H), 7.02 (s, 1H), 6.84 (s, 1H), 6.57 (br s, 1H).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08829185B2uspto-grants-2014_09