تفاعل #84859

ord-f609b59992724aee8797401bfcc1186f

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىThe mixture was placed under a drying tube
  2. 2
    workup.STIRRINGthe mixture stirred for 24 hrs more
  3. 3
    أخرىThe layers were separated
  4. 4
    استخلاصthe aqueous layer was extracted with CH2Cl2
  5. 5
    غسيلThe combined organics were washed with brine
  6. 6
    تجفيفdried over MgSO4
  7. 7
    تركيزconcentrated in vacuo
  8. 8
    أخرىPurification by chromatography (20-35% EtOAc-hexanes containing 1% Et3N)

الإجراء التجريبي

To a solution of 2-hydroxy-3-methoxy-3-(4-morpholinophenyl)propanenitrile (˜5.1 mmol) in anhydr CH2Cl2 (17 mL) under argon was added pyridinium para-toluenesulfonate (0.094 g, 0.37 mmol) and ethyl vinyl ether (17 mL, 178 mmol). The mixture was placed under a drying tube and stirred at room temperature for 16 hrs. Additional ethylvinyl ether (4 mL, 42 mmol) and pyridinium para-toluenesulfonate (0.11 g, 0.44 mmol) were added and the mixture stirred for 24 hrs more. Saturated aqueous NaHCO3 was added to the mixture then it was diluted with H2O and CH2Cl2. The layers were separated and the aqueous layer was extracted with CH2Cl2. The combined organics were washed with brine, dried over MgSO4 and concentrated in vacuo. Purification by chromatography (20-35% EtOAc-hexanes containing 1% Et3N) gave 2-(1-ethoxyethoxy)-3-methoxy-3-(4-morpholinophenyl)propanenitrile (0.606 g, 35% for three steps).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US09434707B2uspto-grants-2016_09