تفاعل #1499
ord-62dac6c13c4c4aa59ca7877a94095e3c
معادلة التفاعل
1-(4-fluorophenyl)-4-(trans-4-pentyl-4-silacyclohexyl)-1-butyne-3-ol
p-toluenesulfonic acid monohydrate
→
desired product
المردود 15.9%
1-(4-flurophenyl)-4-(trans-4-pentyl-4-silacyclohexyl)-3E-butene-1-yne
المردود 15.9%
المتفاعلات
الكواشف
لا شيء
المذيبات
ظروف التفاعل
الظروف التفصيلية
See reaction.notes.procedure_details.
المعالجة
- 1درجة الحرارةwas heated
- 2درجة الحرارةunder reflux
- 3أخرىto remove the water
- 4أخرىThe reaction mixture thus obtained
- 5workup.ADDITIONa mixture of trans- and cis-isomers
- 6workup.ADDITIONwith respect to the silacyclohexane ring, but also a mixture of E- and Z-isomers
- 7أخرىHence, the product was separated by chromatography
الإجراء التجريبي
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%).