Реакция #77716

ord-e2efc53ca1894beeb3afa35c33fbafd0

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Промывкаwashed with 5% HCl (20 mL)
  2. 2
    СушкаThe organic layer was dried over MgSO4
  3. 3
    Фильтрацияfiltered
  4. 4
    Концентрированиеconcentrated
  5. 5
    ДругоеThe residue was purified via flash chromatography

Методика

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).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US06706740B2uspto-grants-2004_03