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Method for production of hydroxyalkylglycol ethers

Assignee: Henkel AG and Co KGaA
•
Filing: 1974-04-08
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Granted: 1976-01-06
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Expires: 1994-04-08
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Abstract

Abstract A method for the production of hydroxyalkyl glycol ethers comprises reacting non-terminal epoxides with ethylene glycol in the presence of an alkoxylation catalyst and saturated hydrocarbons, in particular, saturated aliphatic hydrocarbons, as solvents.

Inventors

  • 👤 Wolfgang Rupilius

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-28 09:17
CPC Classifications
C; C07; C07C; C07C41/00; C07C41/01; C07C41/02; C07C43/00; C07C43/02; C07C43/03; C07C43/04; C07C43/10; C07C43/13

Claims Analysis

Total Claims: 8
Claim 1
Independent Claim 111 words
In the method for the production of hydroxyalkylglycol ethers of the formula ##EQU12## wherein R 1 and R 2 are each alkyl having 2 to 22 carbon atoms, with the proviso that the sum of R 1 plus R 2 is from 6 to 26 carbon atoms, comprising reacting a vicinal non-terminal epoxide of the formula ##EQU13## wherein R 1 and R 2 have the above-defined meanings with ethylene glycol in the presence of a catalytic amount of an acid alkoxylation catalyst; wherein the improvement comprises conducting said reaction in the presence of at least one solvent consisting essentially of at least one saturated hydrocarbon having 4 to 24 carbon atoms.
Claim 2
Dependent Claim 111 words
In the method for the production of hydroxyalkylglycol ethers of the formula ##EQU12## wherein R 1 and R 2 are each alkyl having 2 to 22 carbon atoms, with the proviso that the sum of R 1 plus R 2 is from 6 to 26 carbon atoms, comprising reacting a vicinal non-terminal epoxide of the formula ##EQU13## wherein R 1 and R 2 have the above-defined meanings with ethylene glycol in the presence of a catalytic amount of an acid alkoxylation catalyst; wherein the improvement comprises conducting said reaction in the presence of at least one solvent consisting essentially of at least one saturated hydrocarbon having 4 to 24 carbon atoms.
Claim 3
Dependent Claim 37 words
The method of claim 1, in which said solvent is selected from the group consisting of alkane having 4 to 24 carbon atoms and mixtures thereof and cycloalkane having 4 to 24 carbon atoms and mixtures thereof.
Claim 4
Dependent Claim 37 words
The method of claim 1, in which said solvent is selected from the group consisting of alkane having 5 to 16 carbon atoms, and mixtures thereof and cycloalkane having 5 to 16 carbon atoms and mixtures thereof.
Claim 5
Dependent Claim 37 words
The method of claim 1, in which said solvent is selected from the group consisting of cyclohexane, cyclopentane, decahydronaphthalene and mixtures thereof and pentane, hexane, heptane, octane, nonane, decane, undecane, dodecane, tridecane, pentadecane, hexadecane, and mixtures thereof.
Claim 6
Dependent Claim 24 words
The method of claim 1, in which said solvent is selected from the group consisting of pentane, hexane, heptane, octane and the mixtures thereof.
Claim 7
Dependent Claim 17 words
The method of claim 1, in which said solvent is alkane having 5 to 8 carbon atoms.
Claim 8
Dependent Claim 11 words
The method of claim 1, in which said solvent is pentane.

References Cited (Backward Citations)

US2723294A Cited
US2782240A Cited
US2807651A Cited
US3240819A Cited
US3242200A Cited
GB1150345A Cited
GB1193924A Cited
US3607778A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1979-01-05 1979-07-07 1980-01-06 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1983-01-05 1983-07-07 1984-01-06 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1987-01-05 1987-07-07 1988-01-06 $7700.00 Window Closed / Lapsed

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