반응 #1499

ord-62dac6c13c4c4aa59ca7877a94095e3c

반응 방정식

CCCCC[Si@H]1CC[C@H](CC(O)C#Cc2ccc(F)cc2)CC1
1-(4-fluorophenyl)-4-(trans-4-pentyl-4-silacyclohexyl)-1-butyne-3-ol
Cc1ccc(S(=O)(=O)O)cc1.O
p-toluenesulfonic acid monohydrate
CCCCC[Si@H]1CC[C@H](/C=C/C#Cc2ccc(F)cc2)CC1
desired product
수율 15.9%
CCCCC[Si@H]1CC[C@H](/C=C/C#Cc2ccc(F)cc2)CC1
1-(4-flurophenyl)-4-(trans-4-pentyl-4-silacyclohexyl)-3E-butene-1-yne
수율 15.9%

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도was heated
  2. 2
    온도under reflux
  3. 3
    기타to remove the water
  4. 4
    기타The reaction mixture thus obtained
  5. 5
    workup.ADDITIONa mixture of trans- and cis-isomers
  6. 6
    workup.ADDITIONwith respect to the silacyclohexane ring, but also a mixture of E- and Z-isomers
  7. 7
    기타Hence, the product was separated by chromatography

실험 절차

A mixture of 1-(4-fluorophenyl)-4-(trans-4-pentyl-4-silacyclohexyl)-1-butyne-3-ol 8.0 g (24 mmol), p-toluenesulfonic acid monohydrate 1.6 g, and benzene 200 ml was heated under reflux to remove the water and then subjected to a conventional post-treatment. The reaction mixture thus obtained was not only a mixture of trans- and cis-isomers, with respect to the silacyclohexane ring, but also a mixture of E- and Z-isomers, with respect to the double bond. Hence, the product was separated by chromatography to give 1.2 g of the desired product of the trans-E isomer (yield 15.9%).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05725797uspto-grants-1998_03