تفاعل #65944

ord-8b2516d2034544ccbbfac83330c4c545

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.WAITthe stirring continued at 90° C. for 17 h
  2. 2
    أخرىThe volatiles were evaporated
  3. 3
    غسيلAfter washing with 10% acetic acid (1×30 mL) and 2M ammonia (1×30 mL) the solution
  4. 4
    تجفيفwas dried (MgSO4)
  5. 5
    ترشيحfiltered
  6. 6
    تركيزconcentrated in vacuo
  7. 7
    أخرىto give a brown oil
  8. 8
    غسيلFlash-chromatography of the crude product on a silica column eluted with ethyl acetate /toluene (3:97)

الإجراء التجريبي

8-Fluoro-5-methoxychroman-3-yl carboxylic acid (1.12 g; 85.0 mmol), diphenyl phosphoryl azide (1.3 mL; 5.9 mmol) and toluene (10 mL) were mixed in a three-necked round-bottom flask (50 mL) under nitrogen. Triethylamine (0.83 mL; 5.9 mmol) was added and clear solution was stirred at 100° for 2 h. Benzylalcohol (0.61 mL; 5.9 mmol) was added in one portion and the stirring continued at 90° C. for 17 h. The volatiles were evaporated and the residue was taken up in toluene (25 mL). After washing with 10% acetic acid (1×30 mL) and 2M ammonia (1×30 mL) the solution was dried (MgSO4), filtered and concentrated in vacuo to give a brown oil. Flash-chromatography of the crude product on a silica column eluted with ethyl acetate /toluene (3:97) afforded compound as an oil (contaminated with 2% unreacted isocyanate according to GC).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05420151uspto-grants-1995_05