Reaktion #5920

ord-d89b6b0a42ba47e2b52fd965ff8e6b9b

Reaktionsgleichung

C=CC(=O)Cl
acryloyl chloride
Clc1ccc(C2CNc3ccccc3S2)cc1
2-(4-chlorophenyl)-3,4-dihydro-2H-1,4-benzothiazine
O=C([O-])O.[Na+]
sodium hydrogen carbonate
O
water
C=CC(=O)N1CC(c2ccc(Cl)cc2)Sc2ccccc21
2-(4-chlorophenyl)-4-acryloyl-3,4-dihyro-2H-1,4-benzothiazine
Ausbeute 93.0%

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.ADDITIONis added dropwise
  2. 2
    Waschenthe organic layer is washed
  3. 3
    Sonstigedried
  4. 4
    workup.DISTILLATIONAfter the solvent is distilled off
  5. 5
    Waschenthe resulting crystals are washed with n-hexane

Vorschrift

To a mixture of 2-(4-chlorophenyl)-3,4-dihydro-2H-1,4-benzothiazine (9.62 g), sodium hydrogen carbonate (6.0 g), methylene chloride (100 ml) and water (50 ml) is added dropwise with stirring a solution of acryloyl chloride (5.0 g) in methylene chloride (20 ml) under ice cooling over a period of about 30 minutes. The mixture is stirred at room temperature for 3 hours, and the organic layer is washed and dried. After the solvent is distilled off, the resulting crystals are washed with n-hexane to give 2-(4-chlorophenyl)-4-acryloyl-3,4-dihyro-2H-1,4-benzothiazine (10.76 g, yield 93%).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05246929uspto-grants-1993_09