反应 #2460358

ord-f1a1c4d892034625be1f4de1d662e73a

反应方程式

Oc1ccc(Br)cc1
4-Bromophenol
[H-].[Na+]
sodium hydride
CC(C)(C)OC(=O)CBr
t-Butylbromoacetate
CC(C)(C)OC(=O)COc1ccc(Br)cc1
tert-butyl(4-bromophenoxy)acetate
收率 82.9%

反应条件

温度
75°CELSIUS
详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    浓缩The reaction was concentrated in vacuo
  2. 2
    其他the residue partitioned between ethyl acetate and water
  3. 3
    洗涤The organic phase was washed with saturated ammonium acetate
  4. 4
    浓缩concentrated in vacuo

实验过程

4-Bromophenol (20.4 g, 118 mmol) dissolved in dry N,N-dimethylformamide was carefully treated with sodium hydride (4 g, 167 mmol). t-Butylbromoacetate (23 g, 118 mmol) was added and the mixture heated to 75° C. for 90 minutes. The reaction was concentrated in vacuo and the residue partitioned between ethyl acetate and water. The organic phase was washed with saturated ammonium acetate and concentrated in vacuo to yield 28.1 g of tert-butyl(4-bromophenoxy)acetate.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07459454B2uspto-grants-2008_12