تفاعل #1826

ord-6c41a6072d6542949567036d24ed5e23

معادلة التفاعل

COC(=O)c1ccc(I)cc1
Methyl 4-iodobenzoate
C#CCO
propargyl alcohol
COC(=O)c1ccc(C#CCO)cc1
pale yellow solid
المردود 83.1%
COC(=O)c1ccc(C#CCO)cc1
Methyl 4-(3-hydroxypropynyl)benzoate
المردود 83.1%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىAt the end of this period, diethylamine was removed by concentration in vacuo
  2. 2
    workup.ADDITIONThe residue was diluted with 200 ml of water
  3. 3
    استخلاصextracted three times with 100 ml of benzene and 75 ml of ethyl acetate
  4. 4
    تجفيفdried over Na2SO4
  5. 5
    تركيزconcentrated in vacuo
  6. 6
    أخرىyielding a brown solid
  7. 7
    أخرىThis crude residue was purified by flash chromatography
  8. 8
    غسيلElution with a 2
  9. 9
    workup.ADDITIONto 1 (V:V) mixture of hexane and ethyl acetate

الإجراء التجريبي

Methyl 4-iodobenzoate (9.0 g, 34.4 mmol) was dissolved in 90 ml of diethylamine. The solution was stirred vigorously and, sequentially, 121 milligrams of bis(triphenylphosphine) palladium chloride and 65 milligrams of cuprous iodide were added, each in a single portion, followed by 1.93 grams of propargyl alcohol. The resultant mixture was stirred for about 20 hours at room temperature in an argon atmosphere. At the end of this period, diethylamine was removed by concentration in vacuo. The residue was diluted with 200 ml of water and extracted three times with 100 ml of benzene and 75 ml of ethyl acetate. The organic extracts were combined, dried over Na2SO4, and concentrated in vacuo, yielding a brown solid. This crude residue was purified by flash chromatography. Elution with a 2 to 1 (V:V) mixture of hexane and ethyl acetate yielded 5.44 grams (83% yield) of a pale yellow solid melting at 81° to 82° C.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05726312uspto-grants-1998_03