反応 #657334

ord-92a8b32be51c464ba385f2f4b6fddb48

反応方程式

CCOC(=O)CBr
ethyl bromoacetate
O=[N+]([O-])c1cc(Br)ccc1O
4-bromo-2-nitro-phenol
O=C([O-])[O-].[K+].[K+]
potassium carbonate
CCOC(=O)COc1ccc(Br)cc1[N+](=O)[O-]
product
収率 77.0%
CCOC(=O)COc1ccc(Br)cc1[N+](=O)[O-]
(4-Bromo-2-nitro-phenoxy)-acetic acid ethyl ester
収率 77.0%

反応条件

温度
60°CELSIUS
詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    温度then cooled to 23° C
  2. 2
    その他The reaction mixture was partitioned between ethyl acetate:heptane (1:1) and water (100 mL each)
  3. 3
    その他The organic layer was separated
  4. 4
    洗浄washed successively with water, saturated brine solution (100 ml
  5. 5
    乾燥each) then dried (MgSO4)
  6. 6
    ろ過filtered
  7. 7
    濃縮concentrated

実験手順

To a solution of 4-bromo-2-nitro-phenol (3.28 g, 15.0 mmol, 1 equiv) in dimethylformamide (40 mL) at 23° C. was added potassium carbonate (4.14 g, 30 mmol, 2 equiv) followed by ethyl bromoacetate (1.84 mL, 16.6 mmol, 1.1 equiv). The resulting mixture was warmed to 60° C. (oil bath) for 90 min then cooled to 23° C. The reaction mixture was partitioned between ethyl acetate:heptane (1:1) and water (100 mL each). The organic layer was separated and washed successively with water, saturated brine solution (100 ml, each) then dried (MgSO4), filtered and concentrated to give 4.50 g (11.5 mmol, 77%) of the product as a yellow oil.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US09023843B2uspto-grants-2015_05