Reaktion #1565

ord-79c673a5defa413ebe1182aa02579411

Reaktionsgleichung

O
water
Cn1c(=O)[nH]c(=O)n(-c2ccc(F)cc2Cl)c1=O
1-(2-chloro-4-fluorophenyl)-3-methyl-s-triazine-2,4,6(1H,3H,5H)-trione
O=C([O-])[O-].[K+].[K+]
potassium carbonate
CC(C)OC(=O)CBr
isopropyl bromoacetate
CC(C)OC(=O)Cn1c(=O)n(C)c(=O)n(-c2ccc(F)cc2Cl)c1=O
title product
Ausbeute 92.4%
CC(C)OC(=O)Cn1c(=O)n(C)c(=O)n(-c2ccc(F)cc2Cl)c1=O
Isopropyl 3-(2-chloro-4-fluorophenyl)tetrahydro-5-methyl-2,4,6-trioxo-s-triazine-1(2H)-acetate
Ausbeute 92.4%

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Extraktionextracted with ethyl acetate
  2. 2
    ExtraktionThe organic extract
  3. 3
    Waschenis washed sequentially with water and brine
  4. 4
    Trocknendried over anhydrous magnesium sulfate
  5. 5
    Einengenconcentrated in vacuo
  6. 6
    Sonstigeto obtain an oil

Vorschrift

A mixture of 1-(2-chloro-4-fluorophenyl)-3-methyl-s-triazine-2,4,6(1H,3H,5H)-trione (40.9 g, 0.150 mol), potassium carbonate (31.1 g, 0.225 mol) and isopropyl bromoacetate (29.1 mL, 0.225 mol) in N,N-dimethylformamide is stirred at room temperature for 2 hours, poured into water and extracted with ethyl acetate. The organic extract is washed sequentially with water and brine, dried over anhydrous magnesium sulfate and concentrated in vacuo to obtain an oil. Flash column chromatography of the oil using silica gel and 0% to 10% ether in methylene chloride solutions gives the title product as a white solid (51.5 g, mp 127°-128° C.).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05726126uspto-grants-1998_03