تفاعل #1098649

ord-f57bf2388139448197404de02ee41f3b

معادلة التفاعل

Cc1ccc(S(=O)(=O)OC2COC(c3ccccc3)OC2)cc1
2-phenyl-1,3-dioxan-5-yl 4-methylbenzenesulfonate
CN(C)C=O
DMF
[N-]=[N+]=[N-].[Na+]
NaN3
[N-]=[N+]=NC1COC(c2ccccc2)OC1
22
المردود 84.1%
[N-]=[N+]=NC1COC(c2ccccc2)OC1
5-Azido-2-phenyl-1,3-dioxane
المردود 84.1%

الكواشف

لا شيء

المذيبات

ظروف التفاعل

درجة الحرارة
105°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    تركيزThe reaction was then concentrated to dryness
  2. 2
    workup.DISSOLUTIONThe solid was dissolved in water (700 mL)
  3. 3
    استخلاصextracted into EtOAc (3×500 mL)
  4. 4
    غسيلThe combined organic layers were washed with water (5×)
  5. 5
    تركيزconcentrated to dryness
  6. 6
    أخرىto afford an orange solid
  7. 7
    أخرىThe material was then recrystallized from hexanes

الإجراء التجريبي

To a 1 L round bottom flask was added 2-phenyl-1,3-dioxan-5-yl 4-methylbenzenesulfonate (40 g, 120 mmol) and DMF (500 mL). NaN3 (31.3 g, 478 mmol) was added as a solution in water (150 mL). The reaction was stirred at 105° C. for 2 days. The reaction was then concentrated to dryness. The solid was dissolved in water (700 mL) and extracted into EtOAc (3×500 mL). The combined organic layers were washed with water (5×) and concentrated to dryness to afford an orange solid. The material was then recrystallized from hexanes to afford 20.7 g (84% yield) of 22 as a pale brown solid. 1H NMR (CDCl3, 400 MHz), δ: 3.67 (2H, pseudo t, J=11.59 Hz), 3.78-3.88 (1H, m), 4.36-4.04 (2H, m), 7.36-7.39 (3H, m), 7.45-7.47 (2H, m). Mass Spec (lo-res): Calc'd for C10H11N3O2: 205.09; found: 178.1 (M+H−N2).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07977361B2uspto-grants-2011_07