Patent US4239911A successfully refreshed from Google Patents.
← Back to Patent Explorer
US4239911A Expired / Lapsed US ⏱️ 0.0 years remaining

Manufacture of glycol esters

Assignee: BASF SE
•
Filing: 1977-05-24
•
Granted: 1980-12-16
•
Expires: 1997-05-24
📄 Original PDF 🌐 Google Patents 🔄 Sync Now

Abstract

Abstract Alkylene glycol dicarboxylates are obtained by reacting carboxylic acid esters of monohydric or polyhydric aliphatic short-chain alcohols with an olefin and oxygen in the presence of a catalyst, a hydrolyzing agent and water.

Inventors

  • 👤 Hans-Martin Weitz
  • 👤 Juergen Hartig

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-29 08:55
CPC Classifications
C; C07; C07C; C07C67/00

Claims Analysis

Total Claims: 7
Claim 1
Independent Claim 135 words
In a one-step liquid phase process for the manufacture of ethylene glycol diformate or diacetate or 1,2-propylene glycol diformate or diacetate by reacting ethylene or propylene, molecular oxygen and the appropriate carboxylic acid in a reaction chamber and in the presence of an effective amount of oxyacylation catalyst containing a compound of a transition metal selected from the group of Te, Ce, Sb, Mn, V, Ga, As and Co in conjuction with a halogen or a hydrohalic acid, the improvement which comprises: using an ester of formic acid or acetic acid with a short-chain aliphatic alcohol of 1-5 carbon atoms in place of the carboxylic acid and carrying out the reaction in the presence of an effective amount of an hydrolysis catalyst and not less than 1 mole of water per mole of olefin converted.
Claim 2
Dependent Claim 135 words
In a one-step liquid phase process for the manufacture of ethylene glycol diformate or diacetate or 1,2-propylene glycol diformate or diacetate by reacting ethylene or propylene, molecular oxygen and the appropriate carboxylic acid in a reaction chamber and in the presence of an effective amount of oxyacylation catalyst containing a compound of a transition metal selected from the group of Te, Ce, Sb, Mn, V, Ga, As and Co in conjuction with a halogen or a hydrohalic acid, the improvement which comprises: using an ester of formic acid or acetic acid with a short-chain aliphatic alcohol of 1-5 carbon atoms in place of the carboxylic acid and carrying out the reaction in the presence of an effective amount of an hydrolysis catalyst and not less than 1 mole of water per mole of olefin converted.
Claim 3
Dependent Claim 19 words
A process as set forth in claim 1, wherein methyl acetate or ethyl acetate is used as the ester.
Claim 4
Dependent Claim 18 words
A process as set forth in claim 1, wherein the glycol ester itself is used as the ester.
Claim 5
Dependent Claim 15 words
A process as set forth in claim 1, wherein the hydrolysis catalyst is an acid.
Claim 6
Dependent Claim 23 words
A process as set forth in claim 1, wherein the oxyacylation is carried out at temperatures of from about 100° to 200° C.
Claim 7
Dependent Claim 23 words
A process as set forth in claim 1, wherein the oxyacylation is carried out at pressures of from about 10 to 200 bars.

References Cited (Backward Citations)

US2497408A Cited
US3755423A Cited
US3965156A Cited
US3965152A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1983-12-16 1984-06-16 1984-12-16 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1987-12-16 1988-06-16 1988-12-16 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1991-12-16 1992-06-16 1992-12-16 $7700.00 Window Closed / Lapsed

Assigned Categories & Tags

No categories assigned to this patent yet.

Assign Category Tag