반응 #1566

ord-3e822e48328449ad872c68dab16e1be0

반응 방정식

O=[N+]([O-])O
nitric acid
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
O=[N+]([O-])O
nitric acid
O=[N+]([O-])O
nitric acid
O=[N+]([O-])O
nitric acid
Cn1c(=O)n(CC(=O)O)c(=O)n(-c2cc([N+](=O)[O-])c(F)cc2Cl)c1=O
title product
Cn1c(=O)n(CC(=O)O)c(=O)n(-c2cc([N+](=O)[O-])c(F)cc2Cl)c1=O
3-(2-Chloro-4-fluoro-5-nitrophenyl)tetrahydro-5-methyl-2,4,6-trioxo-s-triazine-1(2H)-acetic acid

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.STIRRINGstirred for 4 hours
  2. 2
    workup.STIRRINGstirred at room temperature overnight
  3. 3
    workup.STIRRINGstirred for 1 hour
  4. 4
    workup.ADDITIONpoured onto ice
  5. 5
    여과The resultant aqueous solution is filtered
  6. 6
    기타to obtain a solid
  7. 7
    건조A solution of the solid in ether is dried over anhydrous magnesium sulfate
  8. 8
    농축concentrated in vacuo

실험 절차

A solution of isopropyl 3-(2-chloro-4-fluorophenyl)tetrahydro-5-methyl-2,4,6-trioxo-s-triazine-1(2H)-acetate (48.7 g, 0.0508 mol) in concentrated sulfuric acid is cooled to 0° C., treated with 90% nitric acid (2.6 mL), stirred at room temperature overnight, treated with 90% nitric acid (1.0 mL), stirred for 4 hours, treated with 90% nitric acid (2.0 mL), stirred at room temperature overnight, treated with 90% nitric acid (1.0 mL), stirred for 1 hour and poured onto ice. The resultant aqueous solution is filtered to obtain a solid. A solution of the solid in ether is dried over anhydrous magnesium sulfate and concentrated in vacuo to give the title product as a yellow foam which is identified by NMR spectral analyses.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05726126uspto-grants-1998_03