Reaktion #217014

ord-40a3b2b9e5c448a0ad925245d4f739eb

Reaktionsgleichung

CCOC(=O)c1cc(C(C)=O)[nH]n1
5-acetylpyrazole-3-carboxylic acid ethyl ester
C1CCOC1
tetrahydrofuran
C[N+](C)(C)c1ccccc1.C[N+](C)(C)c1ccccc1.C[N+](C)(C)c1ccccc1.[Br-].[Br-].[Br-]
phenyltrimethylammonium tribromide
CCOC(=O)c1cc(C(=O)CBr)[nH]n1
5-(2-bromoacetyl)pyrazole-3-carboxylic acid ethyl ester
Ausbeute 145.7%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    FiltrationThe resulting mixture was filtered
  2. 2
    Waschenthe solids were washed with more water
  3. 3
    SonstigeThe solids were collected
  4. 4
    Sonstigeair-dried
  5. 5
    Sonstigerecrystallized from 1:1 mixture of disopropyl ether and hexanes (300ml)

Vorschrift

A 100ml flask was charged with 27.8 g of 5-acetylpyrazole-3-carboxylic acid ethyl ester and 40 ml of tetrahydrofuran. To this mixture, 56.4 g of phenyltrimethylammonium tribromide were added. The resulting red mixture was stirred at room temperature for 1 hour and poured into 600 ml of water. The resulting mixture was filtered and the solids were washed with more water. The solids were collected, air-dried and recrystallized from 1:1 mixture of disopropyl ether and hexanes (300ml) to afford 33.1 g of 5-(2-bromoacetyl)pyrazole-3-carboxylic acid ethyl ester as white solids, mp 174°-176° C. NMR: 1.42 (t, 3H), 4.44 (q, 2H), 4.57 (s, 2H), 7.4 (s, 1H).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05470862uspto-grants-1995_11