تفاعل #992756

ord-5fd85760e2ab442bb81d5387918cffd1

معادلة التفاعل

O=[N+]([O-])c1c(F)cc(F)cc1F
2,4,6-Trifluoronitrobenzene
O=C([O-])[O-].[K+].[K+]
potassium carbonate
C1COCCN1
Morpholine
O=[N+]([O-])c1c(F)cc(N2CCOCC2)cc1F
title compound
المردود 37.0%
O=[N+]([O-])c1c(F)cc(N2CCOCC2)cc1F
4-(3,5-Difluoro-4-nitro-phenyl)-morpholine
المردود 37.0%

الكواشف

لا شيء

المذيبات

ظروف التفاعل

درجة الحرارة
10°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةto warm to 25° C.
  2. 2
    تركيزThe reaction mixture was concentrated in vacuo Brine (50 mL)
  3. 3
    workup.ADDITIONwas added
  4. 4
    استخلاصthe product was extracted with ethyl acetate (3×50 mL)
  5. 5
    تجفيفThe combined organic phases were dried over magnesium sulfate
  6. 6
    تركيزconcentrated in vacuo)
  7. 7
    أخرىThe crude material was purified by flash chromatography

الإجراء التجريبي

2,4,6-Trifluoronitrobenzene (4.95 g) and potassium carbonate (4.63 g) were mixed in dry dimethyl sulfoxide (40 mL) and cooled to 10° C. under argon. Morpholine (2.56 mL) was added and the reaction mixture was allowed to warm to 25° C. and stirred under argon for 16 hours. The reaction mixture was concentrated in vacuo Brine (50 mL) was added and the product was extracted with ethyl acetate (3×50 mL). The combined organic phases were dried over magnesium sulfate and concentrated in vacuo). The crude material was purified by flash chromatography to furnish 2.49 g (37% yield) of the title compound as a yellow solid. 1H NMR (500 MHz, DMSO-d6): 3.43 (t, 4H), 3.69 (t, 4H), 6.87 (d, 2H).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08012962B2uspto-grants-2011_09