Réaction #1869147

ord-817cd11527084050ab0e75f85e5e8e0a

Équation de réaction

Cc1ccccc1C(C#N)=C1SC=CC1=NO
(3-(hydroxy)imino-3H-thiophen-2-ylidene)-(2-methylphenyl)-acetonitrile
CCCS(=O)(=O)Cl
propanesulfonyl chloride
O
water
CCN(CC)CC
triethylamine
CCCS(=O)(=O)ON=C1C=CSC1=C(C#N)c1ccccc1C
yellow crystals
Rendement 70.0%
CCCS(=O)(=O)ON=C1C=CSC1=C(C#N)c1ccccc1C
(3-(propanesulfonyloxy)imino-3H-thiophen-2-ylidene)-(2-methylphenyl)-acetonitrile
Rendement 70.0%

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    TempératureTo the solution cooled
  2. 2
    Autreexceed 10° C
  3. 3
    AutreThe organic layer was separated
  4. 4
    Lavagewashed with 150 g of water three times
  5. 5
    ConcentrationThe organic layer was concentrated in vacuum
  6. 6
    workup.ADDITIONMethanol was added to the
  7. 7
    Concentrationconcentrate for recrystallization
  8. 8
    Filtrationfollowed by filtration
  9. 9
    Autredrying
  10. 10
    AutreThere were obtained crude yellow crystals
  11. 11
    AutreThe crude yellow crystals were purified by silica gel column chromatography (eluent, dichloromethane)
  12. 12
    ConcentrationThe elute was concentrated
  13. 13
    Autrefollowed by recrystallization from methanol, filtration
  14. 14
    Autredrying

Mode opératoire

In 490 g of tetrahydrofuran were dissolved 45 g (0.19 mol) of (3-(hydroxy)imino-3H-thiophen-2-ylidene)-(2-methylphenyl)-acetonitrile in Synthesis Example 1 and 27.0 g (0.19 mol) of commercially available propanesulfonyl chloride. To the solution cooled, 20.6 g (0.20 mol) of triethylamine was added dropwise such that the temperature might not exceed 10° C. The solution was allowed to ripen for 1 hour at room temperature, after which 150 g of water and 500 g of dichloromethane were added. The organic layer was separated, and washed with 150 g of water three times. The organic layer was concentrated in vacuum. Methanol was added to the concentrate for recrystallization, followed by filtration and drying. There were obtained crude yellow crystals. The crude yellow crystals were purified by silica gel column chromatography (eluent, dichloromethane). The elute was concentrated, followed by recrystallization from methanol, filtration and drying. There was obtained 77 g of yellow crystals (yield 70%).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US07498126B2uspto-grants-2009_03