反应 #2171081

ord-fc6fbccb965540f7b6539c1546cf8e9a

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他Volatile material was removed by evaporation
  2. 2
    其他the residue was partitioned between saturated sodium bicarbonate (100 ml) and ethyl acetate (100 ml)
  3. 3
    其他The organic layer was separated
  4. 4
    洗涤washed with saturated sodium chloride (2×100 ml)
  5. 5
    其他dried
  6. 6
    浓缩Concentration

实验过程

4-(2,3-Epoxypropoxy)nitrobenzene (obtained as described in Synthetic Communications, 1994, 24, 833; 4.3 g) was dissolved in methanol (30 ml) and DMF (10 ml). A solution of dimethylamine in methanol (2M, 17 ml) was added and the mixture was stirred overnight. Volatile material was removed by evaporation and the residue was partitioned between saturated sodium bicarbonate (100 ml) and ethyl acetate (100 ml). The organic layer was separated and washed with saturated sodium chloride (2×100 ml) and dried. Concentration gave the product as an oil that slowly crystallised under high vacuum (4.79 g, 89.9%). NMR (CDCl3): 2.33 (s, 6H), 2.98 (m, 1H), 2.54 (m, 1H), 4.00 (m, 3 H), 7.00 (d, 2H), 8.20 (d, 2H); MS (MH+): 241.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US06716831B1uspto-grants-2004_04