تفاعل #927261

ord-e21118d2c93f4115a629f2705b287859

معادلة التفاعل

CCCCCC1(Br)CC1(Br)Br
1,1,2-tribromo-2-pentyl-cyclopropane
[Li][CH2]CCC
n-butyllithium
CN(C)CCN(C)C
tetramethylethylene diamine
CCC=CCBr
1-bromo-2-pentene
CCC=CCC1=C(CCCCC)C1
1-pent-2-enyl-2-pentyl-cyclopropene
المردود 39.1%

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةTo this mixture, cooling in an ice water bath
  2. 2
    workup.WAITfor three hours at room temperature
  3. 3
    استخلاصThis residue was extracted with diethyl ether
  4. 4
    أخرىThe resulting mixture was transferred to a separatory funnel
  5. 5
    أخرىthe phases were separated
  6. 6
    تجفيفThe organic layer was dried over MgSO4
  7. 7
    ترشيحfiltered
  8. 8
    أخرىThe solvent was removed from the filtrate in vacuo

الإجراء التجريبي

A solution of 1.00 g (0.00287 mol) of 1,1,2-tribromo-2-pentyl-cyclopropane in 4 ml of tetrahydrofuran was placed under an inert atmosphere of nitrogen via a Firestone valve. To this mixture, cooling in an ice water bath, was added via syringe 3.58 ml (0.00861 mol) of 1.6M n-butyllithium in hexanes. After 30 minutes, 0.432 ml (0.00287 mol) of tetramethylethylene diamine and 0.339 ml (0.00287 mol) of 1-bromo-2-pentene were added by syringe. The reaction stirred for one hour while warming to room temperature, then for three hours at room temperature. To the resulting mixture was added 2 ml of water. This residue was extracted with diethyl ether. The resulting mixture was transferred to a separatory funnel and the phases were separated. The organic layer was dried over MgSO4 and filtered. The solvent was removed from the filtrate in vacuo to yield 0.200 g (39.1% of theory) of 1-pent-2-enyl-2-pentyl-cyclopropene as an oil.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US06365549B2uspto-grants-2002_04