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

HRID 891243Notes

Reaction equation

HRID 891243 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 (DMSO-d6) δ: 4.56 (t, 1 OH), 3.60–3.35 (m, 36, 18 OCH2), 3.22 (s, 3, 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-a92d681848b34242ac9ffcbf56667ac7
Source dataset
uspto-grants-2006_02
Patent number
US07002012B2

Reaction notes

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