تفاعل #411013

ord-8f34f6f247ae44e380591dc60b11e3d8

معادلة التفاعل

CCCCCCCCBr
1-bromooctane
[Na+].c1cc[cH-]c1
sodium cyclopentadienide
O
water
CCOCC
diethyl ether
CCCCCCCCC1=CC=CC1
n-octylcyclopentadiene
المردود 79.0%

الكواشف

لا شيء

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.ADDITIONwas added
  2. 2
    أخرىThe diethyl ether layer was separated
  3. 3
    تجفيفdried over anhydrous magnesium sulfate
  4. 4
    أخرىAfter removing magnesium sulfate
  5. 5
    workup.DISTILLATIONthe organic solvent was distilled off under a reduced pressure

الإجراء التجريبي

Under a high purity nitrogen atmosphere, 5.8 ml(30mmol) of 1-bromooctane was introduced into a Schlenck flask and 50 ml of tetrahydrofuran (THF) was added thereto. To the resulting mixture, 18 ml of 2N sodium cyclopentadienide in THF was added at 0° C. The resultant was stirred for 5 hours at room temperature, 100 ml of water and 100 ml of diethyl ether were added thereto, followed by agitation. The diethyl ether layer was separated and dried over anhydrous magnesium sulfate. After removing magnesium sulfate, the organic solvent was distilled off under a reduced pressure and the residue was subjected to silica gel column chromatography (eluent: hexane) to obtain 4.21 g of n-octylcyclopentadiene (yield: 79%).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US06214953B1uspto-grants-2001_04