Reaktion #904

ord-9750ebabdd9f4e72aa5a98408ce4247f

Reaktionsgleichung

N
ammonia
O
water
COC(=O)c1c(S(=O)(=O)Cl)ccc([N+](=O)[O-])c1C
2-methoxycarbonyl-3-methyl-4-nitrobenzenesulfonyl chloride
Cc1c([N+](=O)[O-])ccc2c1C(=O)NS2(=O)=O
4-Methyl-5-nitrosaccharin

Lösungsmittel

Reaktionsbedingungen

Temperatur
25°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Einengenthe mixture is concentrated on a rotary evaporator
  2. 2
    Sonstigeto remove water and THF
  3. 3
    workup.STIRRINGThe residue which remains is stirred with ethyl acetate
  4. 4
    Filtrationfiltered off with suction
  5. 5
    Waschenwashed with ethyl acetate
  6. 6
    SonstigeAfter drying under reduced pressure, 34 g (0.131 mol)=79% of theory of a white solid of m.p.: 312° C. (dec.)
  7. 7
    Sonstigeare obtained

Vorschrift

104 ml of 25% ammonia solution are initially taken, 100 ml of water are added and a solution of 48.7 g (0.166 mol) of 2-methoxycarbonyl-3-methyl-4-nitrobenzenesulfonyl chloride in 70 ml of tetrahydrofuran is then added dropwise at 10° C. After stirring at 25° C. for three hours, the mixture is concentrated on a rotary evaporator to remove water and THF. The residue which remains is stirred with ethyl acetate, filtered off with suction and washed with ethyl acetate. After drying under reduced pressure, 34 g (0.131 mol)=79% of theory of a white solid of m.p.: 312° C. (dec.) are obtained.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05723415uspto-grants-1998_03