Glycerol → HCID 75995743, compound

HRID 2369300Notes

Reaction equation

HRID 2369300 reaction equation
[H-].[Na+].[OH:3][CH2:4][CH:5]([CH2:7][OH:8])[OH:6].[CH3:9][C:10]([CH2:26][CH2:27][CH2:28][CH:29]([CH3:36])[CH2:30][CH2:31][CH2:32][CH:33]([CH3:35])[CH3:34])=[CH:11][CH2:12][CH2:13][CH2:14]OS(C1C=CC(C)=CC=1)(=O)=O.O>CN(C)C=O>[CH3:9][C:10]([CH2:26][CH2:27][CH2:28][CH:29]([CH3:36])[CH2:30][CH2:31][CH2:32][CH:33]([CH3:35])[CH3:34])=[CH:11][CH2:12][CH2:13][CH2:14][O:3][CH2:4][CH:5]([CH2:7][OH:8])[OH:6]

Participants

6

Conditions

Temperature
50 °C

Procedure

0.26 g (55%, 5.9 mmol) of sodium hydride was added to a solution of 0.54 g (5.9 mmol) of glycerol in dry N,N-dimethylformamide (6 mL) with cooling on ice. After the mixture was stirred for 30 min at 50° C., the above (5,9,13-trimethyltetradec-4-enyl)tosylate was added dropwise, with additional stirring for 18 hours at the same temperature. After addition of water at 0° C., the reaction mixture was extracted with ethyl acetate. The extract was washed with water, 1M hydrochloric acid, saturated sodium bicarbonate aqueous solution, and saturated brine, successively, and dried over anhydrous sodium sulfate. After filtration, the filtrate was concentrated, and the resulting residue was purified by silica gel column chromatography (ethyl acetate/hexane mixture) to obtain 73 mg of the title compound (6% yield in 2 steps). The results of NMR analysis of the obtained compound are as shown below.

Workup

  1. temperaturewith cooling on ice
  2. stirringwith additional stirring for 18 hours at the same temperature
  3. extractionthe reaction mixture was extracted with ethyl acetate
  4. washThe extract was washed with water, 1M hydrochloric acid, saturated sodium bicarbonate aqueous solution, and saturated brine
  5. dry with materialsuccessively, and dried over anhydrous sodium sulfate
  6. filtrationAfter filtration
  7. concentrationthe filtrate was concentrated
  8. customthe resulting residue was purified by silica gel column chromatography (ethyl acetate/hexane mixture)

Sources & evidence

ORD record
ord-6ebcc6cee3c7400a9e16249c147e6266
Source dataset
uspto-grants-2014_04
Patent number
US08703922B2

Reaction notes

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