تفاعل #1833266

ord-ba45359c84da4b2e94b7ea2b263f81b6

معادلة التفاعل

O
water
C[S+](C)(C)=O.[I-]
Trimethylsulfoxonium iodide
CC(C)(C)O
t-BuOH
O=[N+]([O-])/C=C/c1ccc(OCc2ccccc2)cc1
1-(benzyloxy)-4-[(E)-2-nitrovinyl]benzene
O=[N+]([O-])[C@@H]1C[C@H]1c1ccc(OCc2ccccc2)cc1
1-(benzyloxy)-4-[(trans)-2-nitrocyclopropyl]benzene
المردود 26.0%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    استخلاصextracted with Et2O (3×10 mL)
  2. 2
    غسيلthe organic layers were washed with brine (2×15 mL)
  3. 3
    تجفيفdried over anhydrous Na2SO4
  4. 4
    ترشيحfiltered
  5. 5
    أخرىAfter removal of the solvent
  6. 6
    أخرىthe residual orange oil was purified by column chromatography on silica gel (5% EtOAc/hexanes)

الإجراء التجريبي

Trimethylsulfoxonium iodide (0.62 g, 2.82 mmol) was added in portions to a solution of t-BuOH (0.32 g, 2.82 mmol) in dry DMSO (5 mL). After 10 min a solution of 1-(benzyloxy)-4-[(E)-2-nitrovinyl]benzene (0.60 g, 2.35 mmol) in DMSO (5 mL) was transferred via canula and the mixture was stirred at room temperature for 6 h. The reaction was poured over water (10 mL) and extracted with Et2O (3×10 mL); the organic layers were washed with brine (2×15 mL), dried over anhydrous Na2SO4 and filtered. After removal of the solvent, the residual orange oil was purified by column chromatography on silica gel (5% EtOAc/hexanes) affording 0.16 g of 1-(benzyloxy)-4-[(trans)-2-nitrocyclopropyl]benzene [Rf=0.5 (20% EtOAc/hexanes), white solid, 26% yield].

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US09149447B2uspto-grants-2015_10