Oleoyl chloride → 1,3-O-dioleoyl-2-O-(t-butyldimethylsilyl)glycerol

HRID 724766Notes

Reaction equation

HRID 724766 reaction equation
[Si:1]([O:8][CH:9]([CH2:12][OH:13])[CH2:10][OH:11])([C:4]([CH3:7])([CH3:6])[CH3:5])([CH3:3])[CH3:2].[C:14](Cl)(=[O:32])[CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21]/[CH:22]=[CH:23]\[CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH3:31]>N1C=CC=CC=1>[C:14]([O:11][CH2:10][CH:9]([CH2:12][O:13][C:14](=[O:32])[CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21]/[CH:22]=[CH:23]\[CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH3:31])[O:8][Si:1]([C:4]([CH3:7])([CH3:6])[CH3:5])([CH3:3])[CH3:2])(=[O:32])[CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21]/[CH:22]=[CH:23]\[CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH3:31]

Participants

4

Procedure

In 60 ml of pyridine was dissolved 2.75 g (0.013 mol) of 2-O-(t-butyldimethylsilyl)glycerol, followed by addition of 8.82 g (0.028 mol) of oleoyl chloride under ice-cooling. The reaction was conducted at 50° C. for 15 hours. After completion of the reaction, the solvent was distilled off and the residue was diluted with methylene chloride, washed with saturated aqueous sodium hydrogen carbonate solution, dried, and concentrated. The above procedure provided 1,3-O-dioleoyl-2-O-(t-butyldimethylsilyl)glycerol.

Workup

  1. temperaturecooling
  2. customAfter completion of the reaction
  3. distillationthe solvent was distilled off
  4. additionthe residue was diluted with methylene chloride
  5. washwashed with saturated aqueous sodium hydrogen carbonate solution
  6. customdried
  7. concentrationconcentrated

Sources & evidence

ORD record
ord-d83145372073417bbd172145eebf0d47
Source dataset
uspto-grants-1998_01
Patent number
US05705188

Reaction notes

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