تفاعل #685000

ord-6f2d3ef702cb4506ba7a77f827599314

معادلة التفاعل

[Na+].[OH-]
sodium hydroxide
Cl
hydrochloric acid
O=C(COCCc1ccc2occc2c1)N1CCC(O)C1
2-(2-(1-benzofuran-5-yl)ethoxy)-1-(3-hydroxy-1-pyrrolidinyl)-1-ethanone
O
water
OC1CCN(CCOCCc2ccc3occc3c2)C1
achromatic oil
المردود 72.6%
OC1CCN(CCOCCc2ccc3occc3c2)C1
1-(2-(2-(1-benzofuran-5-yl)ethoxy)ethyl)-3-pyrrolidinol
المردود 72.6%

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.ADDITIONwas added dropwise to the obtained solution
  2. 2
    درجة الحرارةwhile cooling on ice
  3. 3
    درجة الحرارةthe obtained mixture was heated
  4. 4
    درجة الحرارةto reflux for 1 hour
  5. 5
    درجة الحرارةAfter cooling
  6. 6
    أخرىan organic layer was separated
  7. 7
    غسيلThe organic layer was successively washed with water
  8. 8
    تجفيفa saturated saline solution, and then dried over anhydrous magnesium sulfate
  9. 9
    workup.DISTILLATIONThereafter, the solvent was distilled away under a reduced pressure
  10. 10
    أخرىThe residue was purified by column chromatography (eluent; chloroform:methanol=30:1 to 10:1)

الإجراء التجريبي

1.39 g of 2-(2-(1-benzofuran-5-yl)ethoxy)-1-(3-hydroxy-1-pyrrolidinyl)-1-ethanone was dissolved in 14.0 ml of tetrahydrofuran. Thereafter, 14.4 ml of a tetrahydrofuran solution containing a 1 mol/l borane-tetrahydrofuran complex was added dropwise to the obtained solution while cooling on ice, and the obtained mixture was then stirred at a room temperature for 17 hours. Thereafter, 8.0 ml of 6 mol/l hydrochloric acid was added to the reaction mixture, and the obtained mixture was heated to reflux for 1 hour. After cooling, water and ethyl acetate were added to the reaction mixture. The pH of the obtained mixture was adjusted to pH 10 by addition of a 2 mol/l aqueous sodium hydroxide solution, and an organic layer was separated. The organic layer was successively washed with water and a saturated saline solution, and then dried over anhydrous magnesium sulfate. Thereafter, the solvent was distilled away under a reduced pressure. The residue was purified by column chromatography (eluent; chloroform:methanol=30:1 to 10:1), so as to obtain 0.96 g of an achromatic oil product, 1-(2-(2-(1-benzofuran-5-yl)ethoxy)ethyl)-3-pyrrolidinol.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07897594B2uspto-grants-2011_03