Ethanol → HCID 21071823, compound

HRID 1444804Notes

Reaction equation

HRID 1444804 reaction equation
C(O)C.[O:4]=[CH:5][C@@H:6]([C@H:8]([C@@H:10]([C@@H:12]([CH2:14][OH:15])[OH:13])[OH:11])[OH:9])[OH:7].[Sn].[CH2:17](Br)[CH:18]=[CH2:19]>O>[CH2:19]([CH:5]([C@@H:6]([C@H:8]([C@@H:10]([C@@H:12]([CH2:14][OH:15])[OH:13])[OH:11])[OH:9])[OH:7])[OH:4])[CH:18]=[CH2:17]

Participants

6

Conditions

Temperature
60 °C

Procedure

A three liter three-necked round bottom flask, equipped with heating mantle, stirrer, nitrogen inlet, and condensor, was charged with 900 mL of ethanol, 150 mL of water, 180 g (1.00 mole) of D-glucose, 119 g (1.00 mole) of tin powder (−100 mesh), and 121 g (1.00 mole) of allyl bromide. The mixture was stirred and slowly heated at 60° C. The gray suspension was stirred at this temperature for 24 hours, in which time the reaction mixture turned a light yellow color. Heat was removed and the mixture was allowed to cool to room temperature. The reaction was neutralized to pH=7 by adding approximately 200 ml of 5M NaOH aqueous solution. The suspension was filtered to remove solids, and the yellow solution was decolorized with multiple treatments of activated carbon. The activated carbon was removed by filtration, and the solvent was removed by rotary evaporation to isolate a white syrup. Typical yield was 200 g with a threo-erythro ratio of 6:1, based on GC-MS. The 1-allyl sorbitol syrup was used without further purification.

Workup

  1. customA three liter three-necked round bottom flask, equipped
  2. temperaturewith heating mantle, stirrer, nitrogen inlet, and condensor
  3. stirringThe gray suspension was stirred at this temperature for 24 hours, in which time the reaction mixture
  4. temperatureHeat
  5. customwas removed
  6. temperatureto cool to room temperature
  7. additionby adding approximately 200 ml of 5M NaOH aqueous solution
  8. filtrationThe suspension was filtered
  9. customto remove solids
  10. customThe activated carbon was removed by filtration
  11. customthe solvent was removed by rotary evaporation
  12. customto isolate a white syrup
  13. customThe 1-allyl sorbitol syrup was used without further purification

Sources & evidence

ORD record
ord-2b8612d1d993431ca754386d9ee5d241
Source dataset
uspto-grants-2010_02
Patent number
US07662978B2

Reaction notes

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