تفاعل #6735

ord-746ede52140b4ff6b3a407b25a39a3df

معادلة التفاعل

[H-].[Na+]
sodium hydride
OCCOCCOCCOCCO
tetraethylene glycol
CS(=O)(=O)[O-]
mesylate
OCCOCCOCCOCCOCc1ccccc1
tetraethylene glycol monobenzylether
OCCOCCOCCOCCOCCOCCOCCOCCOCc1ccccc1
title compound
المردود 34.5%
OCCOCCOCCOCCOCCOCCOCCOCCOCc1ccccc1
Octaethylene Glycol Monobenzylether
المردود 34.5%

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.ADDITIONwas added dropwise
  2. 2
    workup.STIRRINGthe reaction mixture was stirred overnight
  3. 3
    أخرىThe crude reaction mixture
  4. 4
    ترشيحwas filtered through Celite (washed, CH2Cl2, 250 mL)
  5. 5
    غسيلthe filtrate was washed H2O, dried MgSO4
  6. 6
    أخرىevaporated to dryness
  7. 7
    أخرىThe resultant oil was chromatographed (silica, ethyl acetate/methanol, 10:1)
  8. 8
    أخرىchromatographed (silica, chloroform/methanol, 25:1)

الإجراء التجريبي

To a solution of tetrahydrofuran (140 mL) containing sodium hydride (0.43 g, 18 mmol) was added dropwise a solution of non-polydispersed tetraethylene glycol (3.5 g, 18 mmol) in tetrahydrofuran (10 mL) and the reaction mixture was stirred for 1 h. Then mesylate of non-polydispersed tetraethylene glycol monobenzylether 40 (6.0 g, 16.5 mmol) dissolved in tetrahydrofuran (10 mL) was added dropwise and the reaction mixture was stirred overnight. The crude reaction mixture was filtered through Celite (washed, CH2Cl2, 250 mL) and the filtrate was washed H2O, dried MgSO4, and evaporated to dryness. The resultant oil was chromatographed (silica, ethyl acetate/methanol, 10:1) and chromatographed (silica, chloroform/methanol, 25:1) to afford the non-polydispersed title compound as a clear oil (2.62 g, 34% yield).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07084121B2uspto-grants-2006_08