Reaktion #2336522

ord-b042792eae154febbebc73d32bd28eb2

Reaktionsgleichung

Cc1ccccc1S(=O)(=O)Cl
Toluenesulfonyl chloride
CC1COc2cc(-c3ccco3)ccc2C1=NO
7-furyl-3-methyl-4-chromanone oxime
c1ccncc1
pyridine
Cc1ccccc1S(=O)(=O)ON=C1c2ccc(-c3ccco3)cc2OCC1C
7-furyl-3-methyl-4-chromanone O-(toluenesulfonyl)-oxime
Ausbeute 57.1%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Waschenwashed with 5% HCl (20 mL)
  2. 2
    TrocknenThe organic layer was dried over MgSO4
  3. 3
    Filtrationfiltered
  4. 4
    Einengenconcentrated
  5. 5
    SonstigeThe residue was purified via flash chromatography

Vorschrift

Toluenesulfonyl chloride (397 mg, 2.08 mmol) was added to a 0° C. solution of 7-furyl-3-methyl-4-chromanone oxime (61) (461 mg, 1.89 mmol) and pyridine (0.5 mL) in CH2Cl2 (10 mL). After 6 hours, the mixture was diluted with CH2Cl2 (30 mL) and washed with 5% HCl (20 mL). The organic layer was dried over MgSO4, filtered and concentrated. The residue was purified via flash chromatography using 5:1 hexanes:EtOAc as the eluent, to provide 7-furyl-3-methyl-4-chromanone O-(toluenesulfonyl)-oxime (62) (429 mg) as a pink solid, m.p. 163-164° C. (dec).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: USRE039991E1uspto-grants-2008_01