Glycerol → 1-O-pentyl-glycerol ether

HRID 1404751

反応式

HRID 1404751 の反応式
[OH:1][CH2:2][CH:3]([CH2:5][OH:6])[OH:4].[C:7]([OH:13])(=O)[CH2:8][CH2:9][CH2:10][CH3:11]>[Pd]>[CH2:7]([O:1][CH2:2][CH:3]([CH2:5][OH:6])[OH:4])[CH2:8][CH2:9][CH2:10][CH3:11].[CH3:2][CH2:3][O:13][CH2:7][CH3:8]

参加物

4

反応条件

温度
120 °C

実験手順

A stirred autoclave was charged, at room temperature, with the mixture of catalysts recycled from example 31 (AMBERLYST® (a polymer based catalyst) 35 and Pd/C), with 65.56 g (712 mmol) of glycerol and 1.80 g (17.6 mmol) of valeric acid. 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 filtered on a MILLIPORE® filter (a membrane filter) (0.1 μm) and was rinsed with absolute ethanol. The solvents were 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 (2×30 ml) and the CH2Cl2 was then evaporated at reduced pressure. The crude reaction product was purified on a flash silica column (eluent: cyclohexane/ethyl acetate=4:1˜1:1). 1-O-pentyl-glycerol ether was obtained at an isolated yield of 72%.

後処理

  1. additionA stirred autoclave was charged, at room temperature, with the mixture of catalysts
  2. customAfter 16 h of reaction
  3. customwas brought back to room temperature
  4. filtrationThe catalyst was filtered on a MILLIPORE®
  5. filtrationfilter (a membrane
  6. filtrationfilter) (0.1 μm)
  7. washwas rinsed with absolute ethanol
  8. customThe solvents were evaporated
  9. extractionthe organic products were extracted from the glycerol phase by extraction with CH2Cl2 (3×50 ml)
  10. washThe organic phase was washed with water (2×30 ml)
  11. customthe CH2Cl2 was then evaporated at reduced pressure
  12. customThe crude reaction product
  13. customwas purified on a flash silica column (eluent: cyclohexane/ethyl acetate=4:1˜1:1)

出典と根拠

ORDレコード
ord-96259fd8ff174ce5bb7b422097f99a06
出典データセット
uspto-grants-2014_12
特許番号
US08912365B2

関連ノート

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