1-Phenyl-2,5,8,11,14,17,20,23,26,29-decaoxatriacontane → Nonaethylene Glycol Monomethyl Ether

HRID 396265Notes

Reaction equation

HRID 396265 reaction equation
C[O:2][CH2:3][CH2:4][O:5][CH2:6][CH2:7][O:8][CH2:9][CH2:10][O:11][CH2:12][CH2:13][O:14][CH2:15][CH2:16][O:17][CH2:18][CH2:19][O:20][CH2:21][CH2:22][O:23][CH2:24][CH2:25][O:26][CH2:27][CH2:28][O:29][CH2:30]C1C=CC=CC=1>C(O)C.[Pd]>[CH3:30][O:29][CH2:28][CH2:27][O:26][CH2:25][CH2:24][O:23][CH2:22][CH2:21][O:20][CH2:19][CH2:18][O:17][CH2:16][CH2:15][O:14][CH2:13][CH2:12][O:11][CH2:10][CH2:9][O:8][CH2:7][CH2:6][O:5][CH2:4][CH2:3][OH:2]

Participants

4

Procedure

A solution of nonaethylene glycol benzyl methyl ether (10 g, 19.3 mmol) in ethanol (200 mL) was shaken with 10% palladium on activated charcal (Aldrich, 1.0 g) under hydrogen (50 psi) on a Parr apparatus for 3 h. The catalyst was filtered off (Celite), and the filtrate was concentrated in vacuo and dried by evaporation of toluene to provide nonaethylene glycol monomethyl ether as an oil (8.17 g, 99%). 1H-NMR (300 MHz, DMSO-d6) δ: 4.56 (t, 1H OH), 3.60-3.35 (m, 36H, 18 OCH2), 3.22 (s, 3H, CH3).

Workup

  1. filtrationThe catalyst was filtered off (Celite)
  2. concentrationthe filtrate was concentrated in vacuo
  3. dry with materialdried by evaporation of toluene

Sources & evidence

ORD record
ord-2042dbac3bc3491cb46a8e12331dab92
Source dataset
uspto-grants-2003_08
Patent number
US06608069B1

Reaction notes

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