反応 #640575

ord-279427bedc5d4d239b00cc6dfc2c8131

反応方程式

O=C1OC(c2ccccc2)CCN1Cc1ccccc1[N+](=O)[O-]
3-(2-Nitrobenzyl)-6-phenyl-[1,3]-oxazinan-2-one
[Cl-].[NH4+]
ammonium chloride
O
water
Nc1ccccc1CN1CCC(c2ccccc2)OC1=O
3-(2-aminobenzyl)-6-phenyl-[1,3]-oxazinan-2-one
収率 99.3%

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    温度to reflux for 1.5 hours
  2. 2
    ろ過the reaction mixture was filtered with suction
  3. 3
    抽出extracted with ethyl acetate
  4. 4
    洗浄The organic layer was washed with a saturated brine
  5. 5
    乾燥dried over anhydrous sodium sulfate

実験手順

3-(2-Nitrobenzyl)-6-phenyl-[1,3]-oxazinan-2-one (1.59 g, 5.10 mmol), iron powder (1.42 g, 25.4 mmol), ammonium chloride (0.14 g, 2.62 mmol) were suspended in ethanol (30 ml) and water (15 ml) and heated to reflux for 1.5 hours. After cooling to room temperature, the reaction mixture was filtered with suction and extracted with ethyl acetate. The organic layer was washed with a saturated brine and then dried over anhydrous sodium sulfate, and 3-(2-aminobenzyl)-6-phenyl-[1,3]-oxazinan-2-one (1.43 g) was obtained by evaporating the solvent under reduced pressure.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US08048825B2uspto-grants-2011_11