تفاعل #792184

ord-8c0ad605730944dabba5b4e065da2eb3

معادلة التفاعل

Brc1ccco1
2-bromofuran
CC(C)NC(C)C
diisopropylamine
C1CCOC1
THF
C#C[Si](C)(C)C
trimethylsilyl acetylene
C[Si](C)(C)C#Cc1ccco1
(furan-2-ylethynyl)trimethylsilane
المردود 35.8%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.ADDITIONwas added at room temperature
  2. 2
    استخلاصextracted with dichloromethane
  3. 3
    غسيلThe combined organic layers were washed with brine
  4. 4
    تجفيفdried over anhydrous sodium sulfate
  5. 5
    أخرىthe solvent was evaporated
  6. 6
    أخرىThe crude material was purified by column chromatography (100-200 mesh silica gel)

الإجراء التجريبي

A mixture of 2-bromofuran (500 mg, 3.402 mmol), Pd(PPh3)2Cl2 (75.69 mg, 0.10784 mmol), CuI (40.17 mg, 0.2109 mmol) and diisopropylamine (0.89 ml, 6.395 mmol) in tetrahydrofuaran (THF) (4 ml) was degassed thoroughly with argon, and trimethylsilyl acetylene (0.648 ml, 4.694 mmol) was added at room temperature. After stirring the reaction mixture for 16 hours at room temperature, it was poured into water and extracted with dichloromethane. The combined organic layers were washed with brine and dried over anhydrous sodium sulfate and the solvent was evaporated. The crude material was purified by column chromatography (100-200 mesh silica gel) using hexane as eluent to yield the desired (furan-2-ylethynyl)trimethylsilane (200 mg, 1.21 mmol, yield 35.84%).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US09173401B2uspto-grants-2015_11