Reaction #6717

ord-baeec4a04db444d58f3d0e5cdc22f086

Reaction equation

CCOC(=O)CCCCCOCCOCCOCCOCCOCCOCCOCc1ccccc1
benzyl ether
CCOC(=O)CCCCCOCCOCCOCCOCCOCCOCCOCc1ccccc1
6-{2-[2-(2-{2-[2-(2-Benzyloxyethoxy)ethoxy]ethoxy}-ethoxy)-ethoxy]-ethoxy}-hexanoic acid ethyl ester
CCOC(=O)CCCCCOCCOCCOCCOCCOCCOCCO
title compound
Yield 79.0%
CCOC(=O)CCCCCOCCOCCOCCOCCOCCOCCO
6-{2-[2-(2-{2-[2-(2-hydroxyethoxy)ethoxy]ethoxy}-ethoxy)-ethoxy]-ethoxy}-hexanoic acid ethyl ester
Yield 79.0%

Solvents

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    FiltrationThe reaction mixture was filtered through Celite 545
  2. 2
    Otherto remove the catalyst
  3. 3
    Concentrationthe filtrate was concentrated in vacuo

Procedure

Non-polydispersed benzyl ether 18 (1.03 g, 2.0 mmol) was dissolved in 25 ml ethanol. To this solution was added 270 mg 10% Pd/C, and the mixture was placed under a hydrogen atmosphere and stirred for four hours, at which time TLC showed the complete disappearance of the starting material. The reaction mixture was filtered through Celite 545 to remove the catalyst, and the filtrate was concentrated in vacuo to yield the non-polydispersed title compound as a clear oil (0.67 g, 79%). FAB MS: m/e 425 (M+H), 447 (M+Na).

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07084114B2uspto-grants-2006_08