反応 #8518

ord-dd9e3a31161d42c9b3f9a0536f7ed37e

反応方程式

[Cl-].[Cl-].c1cc(C[S+]2CCCC2)ccc1C[S+]1CCCC1
p-xylylenebis(tetrahydrothiophenium chloride)
CC(C)(C)[O-].[Na+]
sodium t-butoxide
CCCCCCCCS
octanethiol
Cl
hydrochloric acid
CCCCCCCCSCc1ccc(CSCCCCCCCC)cc1
p-bis(octylthiomethyl)benzene
CCCCCCCCSCc1ccc(CCl)cc1
p-(Octylthiomethyl)benzyl chloride

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    workup.WAITAfter one hour
  2. 2
    その他all the volatile components were removed under reduced pressure
  3. 3
    ろ過the undissolved constituents were filtered off
  4. 4
    その他the filtrate was evaporated under reduced pressure
  5. 5
    workup.ADDITIONThe oil was mixed with twice the volume of octane
  6. 6
    workup.DISTILLATIONdistilled off under reduced pressure together with tetrahydrothiophene
  7. 7
    その他finally giving 5.31 g

実験手順

1.83 g (19 mmol) of sodium t-butoxide and 2.78 g (19 mmol) of octanethiol were stirred into 40 g of methanol at room temperature. After 30 minutes, the clear solution was added in one portion to 6.68 g (19 mmol) of the p-xylylenebis(tetrahydrothiophenium chloride) obtained in accordance with Example 1, in 100 g of methanol. After one hour, the mixture was neutralized using 1N hydrochloric acid, and all the volatile components were removed under reduced pressure. The crude product was taken up in 200 ml of chloroform, the undissolved constituents were filtered off, and the filtrate was evaporated under reduced pressure. The oil was mixed with twice the volume of octane, and distilled off under reduced pressure together with tetrahydrothiophene. This sequence was repeated three times with octane, finally giving 5.31 g, consisting of 90% of product, 5% of starting material and 5% of p-bis(octylthiomethyl)benzene. This reaction was carried out at various temperatures and the product distribution analyzed by 1H-NMR spectroscopy (all data in mol-%).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US07087787B1uspto-grants-2006_08