Реакция #640574

ord-ef7b56bbb7c4465581475e06a2593128

Уравнение реакции

O
water
O=[N+]([O-])c1ccccc1CNCCC(O)c1ccccc1
3-(2-Nitrobenzylamino)-1-phenylpropanol
CCN(CC)CC
triethylamine
O=C(OC(Cl)(Cl)Cl)OC(Cl)(Cl)Cl
triphosgene
O=C1OC(c2ccccc2)CCN1Cc1ccccc1[N+](=O)[O-]
3-(2-nitrobenzyl)-6-phenyl-[1,3]-oxazinan-2-one
Выход 129.9%

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    workup.ADDITIONwas slowly added dropwise
  2. 2
    Температураheated
  3. 3
    Температураto reflux for six hours
  4. 4
    Температураto cool
  5. 5
    Экстракцияextracted with ethyl acetate
  6. 6
    ПромывкаThe organic layer was washed with 0.1N hydrochloric acid water
  7. 7
    Сушкаdried over anhydrous sodium sulfate
  8. 8
    Другоеthe solvent was evaporated under reduced pressure
  9. 9
    ПромывкаThe residue was washed with a mixture of ether-ethyl acetate (1:2)

Методика

3-(2-Nitrobenzylamino)-1-phenylpropanol (3.00 g, 10.5 mmol), triethylamine (4.24 g, 42.0 mmol) were dissolved in toluene (50 ml). Under ice cooled condition, a solution in which triphosgene (1.24 g, 4.19 mmol) was dissolved in toluene (5 ml) was slowly added dropwise thereto and heated to reflux for six hours after stirred at room temperature for one hour. The reaction mixture was poured into water and, after standing to cool, extracted with ethyl acetate. The organic layer was washed with 0.1N hydrochloric acid water and then dried over anhydrous sodium sulfate and the solvent was evaporated under reduced pressure. The residue was washed with a mixture of ether-ethyl acetate (1:2) to obtain 3-(2-nitrobenzyl)-6-phenyl-[1,3]-oxazinan-2-one (1.70 g).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US08048825B2uspto-grants-2011_11