تفاعل #82549

ord-5265c609d750480b8b3ec7e1eb63a113

معادلة التفاعل

O
water
[Li][CH2]CCC
n-butyllithium
CC(C)(C=CI)c1ccc(Cl)cc1
3-methyl-3-(4-chlorophenyl)-1-iodo-1-butene
[CH3][Sn]([CH3])([CH3])[Cl]
trimethyltin chloride
CC(C)(C=[CH][Sn]([CH3])([CH3])[CH3])c1ccc(Cl)cc1
3-methyl-3-(4-chlorophenyl)-1-trimethylstannyl-1-butene
المردود 87.3%

ظروف التفاعل

درجة الحرارة
-90°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةto maintain the reaction mixture temperature at about -85° to -90° C
  2. 2
    workup.ADDITIONUpon completion of the addition
  3. 3
    درجة الحرارةto maintain the reaction mixture temperature at about -85° to -90° C
  4. 4
    workup.ADDITIONUpon completion of addition
  5. 5
    workup.STIRRINGthe reaction mixture is again stirred at -90° C. for 30 minutes
  6. 6
    درجة الحرارةto warm to ambient temperature where it
  7. 7
    workup.STIRRINGis stirred for about 18 hours
  8. 8
    استخلاصextracted with 150 mL of diethyl ether
  9. 9
    استخلاصThe ether extract
  10. 10
    تجفيفis dried with magnesium sulfate
  11. 11
    ترشيحfiltered
  12. 12
    تركيزThe filtrate is concentrated under reduced pressure

الإجراء التجريبي

A stirring solution of 4.8 grams (0.016 mole) of 3-methyl-3-(4-chlorophenyl)-1-iodo-1-butene in 50 mL of tetrahydrofuran is cooled to about -90° C., and 6.9 mL (0.01 8 mole) of n-butyllithium (2.5M in hexane) is added dropwise at a rate to maintain the reaction mixture temperature at about -85° to -90° C. Upon completion of the addition, the reaction mixture is stirred at -90° C. for 30 minutes. After this time, a solution of 3.7 grams (0.019 mole) of trimethyltin chloride in 10 mL of tetrahydrofuran is added dropwise at a rate sufficient to maintain the reaction mixture temperature at about -85° to -90° C. Upon completion of addition, the reaction mixture is again stirred at -90° C. for 30 minutes. After this time, the reaction mixture is allowed to warm to ambient temperature where it is stirred for about 18 hours. The reaction mixture is then poured into 150 mL of water and extracted with 150 mL of diethyl ether. The ether extract is dried with magnesium sulfate and filtered. The filtrate is concentrated under reduced pressure, yielding 4.8 grams of 3-methyl-3-(4-chlorophenyl)-1-trimethylstannyl-1-butene. The NMR spectrum is consistent with the proposed structure.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05622954uspto-grants-1997_04