反応 #1358983

ord-79d8fae2a5d94f4297f25aa2bf94bab9

反応方程式

CN(C)C=O
DMF
O=C1CCC(=O)N1Br
NBS
CCCCC(CC)COc1ccccc1OCC(CC)CCCC
1b
CCCCC(CC)COc1ccccc1OCC(CC)CCCC
1,2-di(2-ethylhexyloxy)benzene
O=C1CCC(=O)N1Br
NBS
CCCCC(CC)COc1ccc(Br)cc1OCC(CC)CCCC
4-bromo-1,2-di(2-ethylhexyloxy)benzene
収率 96.0%

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    洗浄The organic layer was washed with a saturated LiCl solution and water
  2. 2
    乾燥After drying with MgSO4 the solvent
  3. 3
    その他was removed under reduced pressure
  4. 4
    workup.DISTILLATIONThe remaining oil was distilled (160° C./0.01 mmHg)

実験手順

Solid NBS (26.21 g, 0.147 mol) was added to an ice cold CH2Cl2 solution (250 mL) of 1b under N2 in the absence of light. Just enough DMF was added (30 mL) to disolve the NBS. The reaction mixture was allowed to warm to room temperature and then stirred for 12 h. The mixture was then poured into water. The organic layer was washed with a saturated LiCl solution and water. After drying with MgSO4 the solvent was removed under reduced pressure. The remaining oil was distilled (160° C./0.01 mmHg) to yield 4-bromo-1,2-di(2-ethylhexyloxy)benzene (2b) in 96% yield as a colorless oil.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US07208122B2uspto-grants-2007_04