反応 #834827

ord-2e528ec8e55d48bc96199c532db46ee0

反応方程式

C=COCCCl
Chloroethyl vinyl ether
Cc1cc([S+](c2ccc(C(C)(C)C)cc2)c2ccc(C(C)(C)C)cc2)cc(C)c1O.O=S(=O)([O-])C(F)(F)C(F)(F)C(F)(F)C(F)(F)F
4-Hydroxy-3,5-dimethylphenyldi(4-t-butylphenyl)sulfonium perfluorobutanesulfonate salt
O=C([O-])[O-].[K+].[K+]
potassium carbonate
CN(C)CCN(C)C
N,N,N′,N′-tetramethylethylenediamine
C=COCCOc1c(C)cc([S+](c2ccc(C(C)(C)C)cc2)c2ccc(C(C)(C)C)cc2)cc1C.O=S(=O)([O-])C(F)(F)C(F)(F)C(F)(F)C(F)(F)F
4-vinyloxyethoxy-3,5-dimethylphenyldi(4-t-butylphenyl)sulfonium perfluorobutanesulfonate salt

反応条件

温度
80°CELSIUS
詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    温度cooled to 30° C.
  2. 2
    その他After removal of solid
  3. 3
    ろ過through filtration, water (20.9 g)
  4. 4
    workup.ADDITIONwas added to the filtrate
  5. 5
    洗浄the aqueous layer was washed three times with hexane (85.1 g)
  6. 6
    workup.ADDITIONTo the washed aqueous layer, dichloromethane (226 g) and water (141 g) were added
  7. 7
    workup.STIRRINGunder stirring
  8. 8
    抽出whereby the target substance was extracted to the dichloromethane layer
  9. 9
    洗浄The organic layer was repeatedly washed with distilled water until the pH of the separated aqueous layer
  10. 10
    その他The solvent was removed by means of a rotary evaporator

実験手順

4-Hydroxy-3,5-dimethylphenyldi(4-t-butylphenyl)sulfonium perfluorobutanesulfonate salt (28.6 g), potassium carbonate (8.10 g), and N,N,N′,N′-tetramethylethylenediamine (0.46 g) were dissolved in dimethyl sulfoxide (142 g). Chloroethyl vinyl ether (6.08 g) was added to the solution, followed by heating to 80° C. The reaction mixture was stirred for 19 hours and cooled to 30° C. or lower. After removal of solid through filtration, water (20.9 g) was added to the filtrate, and the aqueous layer was washed three times with hexane (85.1 g). To the washed aqueous layer, dichloromethane (226 g) and water (141 g) were added under stirring, whereby the target substance was extracted to the dichloromethane layer. The organic layer was repeatedly washed with distilled water until the pH of the separated aqueous layer was shifted to 7. The solvent was removed by means of a rotary evaporator, to thereby yield 27.4 g of a brown oily substance. Through 1H-NMR and ion chromatography, the substance was identified to be 4-vinyloxyethoxy-3,5-dimethylphenyldi(4-t-butylphenyl)sulfonium perfluorobutanesulfonate salt.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US07396960B2uspto-grants-2008_07