Glycerol → HCID 86708448, compound

HRID 1404738Notes

Reaction equation

HRID 1404738 reaction equation
[OH:1][CH2:2][CH:3]([CH2:5][OH:6])[OH:4].[C:7]([O:14][CH3:15])(=O)[CH2:8][CH2:9][CH2:10][CH2:11][CH3:12]>[Pd]>[CH2:7]([O:1][CH2:2][CH:3]([CH2:5][OH:6])[OH:4])[CH2:8][CH2:9][CH2:10][CH2:11][CH3:12].[CH3:2][CH2:15][O:14][CH2:7][CH3:8]

Participants

4

Conditions

Temperature
120 °C

Procedure

A stirred autoclave was charged, at room temperature, with 65.84 g (715 mmol) of glycerol, 2.29 g (17.6 mmol) of methyl caproate, 0.23 g (10 wt %) of camphosulfonic acid and 0.39 g (1 mol %) of Pd/C at 5%. The autoclave was then pressurized at 50 bar of dihydrogen gas H2, and then it was heated at 120° C. for 16 h, stirring vigorously. After 16 h of reaction, the reaction mixture was brought back to room temperature. The catalyst was then filtered on a MILLIPORE® filter (a membrane filter) (0.45 μm) and was rinsed with absolute ethanol. The solvents were then evaporated and the organic products were extracted from the glycerol phase by extraction with CH2Cl2 (3×50 ml). The organic phase was washed with water (2×20 ml) and the CH2Cl2 was then evaporated at reduced pressure. The crude reaction product was analyzed by GC/MS. 1-O-hexyl-glycerol ether was obtained at 59% GC yield.

Workup

  1. customAfter 16 h of reaction
  2. customwas brought back to room temperature
  3. filtrationThe catalyst was then filtered on a MILLIPORE®
  4. filtrationfilter (a membrane
  5. filtrationfilter) (0.45 μm)
  6. washwas rinsed with absolute ethanol
  7. customThe solvents were then evaporated
  8. extractionthe organic products were extracted from the glycerol phase by extraction with CH2Cl2 (3×50 ml)
  9. washThe organic phase was washed with water (2×20 ml)
  10. customthe CH2Cl2 was then evaporated at reduced pressure
  11. customThe crude reaction product

Sources & evidence

ORD record
ord-3ed80ec44d3c45d7a1fbd58361f875f9
Source dataset
uspto-grants-2014_12
Patent number
US08912365B2

Reaction notes

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