Reaktion #77950

ord-ca4ace3ab43043a2a08b5f0069a97f16

Reaktionsgleichung

Cc1c(Br)ccc(N)c1C1=NOCC1
4-bromo-2-(4,5-dihydroisoxazol-3-yl)-3-methylaniline
Cl
hydrochloric acid
O=S=O
sulfur dioxide
O=N[O-].[Na+]
sodium nitrite
Cc1c(Br)ccc(S(=O)(=O)Cl)c1C1=NOCC1
4-bromo-2-(4,5-dihydroisoxazol-3-yl)-3-methylbenzenesulfonyl Chloride

Reaktionsbedingungen

Temperatur
5°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.STIRRINGThe reaction mixture is stirred at room temperature for 1 hour
  2. 2
    Extraktionextracted with methylene chloride
  3. 3
    WaschenThe organic phase is washed with water
  4. 4
    Trocknendried with magnesium sulfate
  5. 5
    Einengenconcentrated

Vorschrift

At 15° C., a solution of 9 g (35 mmol) of 4-bromo-2-(4,5-dihydroisoxazol-3-yl)-3-methylaniline in 50 ml of glacial acetic acid is added to 15 ml of conc. hydrochloric acid. At 5-10° C., a solution of 2.44 g (35 mmol) of sodium nitrite in 10 ml of water is then added dropwise, and the mixture is stirred at 5° C. for 1 hour. At room temperature, this solution is then added dropwise to a mixture of a solution of 47 g (0.74 mol) of sulfur dioxide in 100 ml of glacial acetic acid and a solution of 2.23 g (13 mmol) of copper(II) chloride in 5 ml of water. The reaction mixture is stirred at room temperature for 1 hour and subsequently poured into 300 ml of ice-water and extracted with methylene chloride. The organic phase is washed with water, dried with magnesium sulfate and concentrated.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US06706886B2uspto-grants-2004_03