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US4187355A Expired / Lapsed US ⏱️ 0.0 years remaining

Production of polyalkylene glycol ethers from formose and use thereof in the preparation of polyurethane resins

Assignee: Bayer AG
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Filing: 1978-08-17
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Granted: 1980-02-05
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Expires: 1998-08-17
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Abstract

Abstract This invention relates to a process for the production of novel polyalkylene glycol ethers based on a mixture of polyhydric alcohols, hydroxyaldehydes and hydroxy ketones produced by the auto-condensation of formaldehyde hydrate (formose). The improvement realized is in the use of an acid catalysis rather than the normal base catalysis. The new polyether polyols are valuable starting materials for the production of polyurethane foams.

Inventors

  • 👤 Kuno Wagner

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-29 18:19
CPC Classifications
C; C08; C08G; C08G18/00; C08G18/06; C08G18/28; C08G18/40; C08G18/48; C08G18/487; C08G18/4883; C07; C07H; C07H15/00; C07H15/02; C07H15/04; C07H15/08; C07H7/00; C07H7/02

Claims Analysis

Total Claims: 13
Claim 1
Independent Claim 86 words
A process for the production of polyether polyols having an average molecular weight of from 200 to 10,000 and an average hydroxyl functionality of from 2.0 to 7.0, comprising reacting one or more cyclic ethers, optionally successively, with a starter comprising: (A) formose which is optionally α-aldolized; or (B) liquid mixtures of: (a) high molecular weight and/or low molecular weight polyhydroxyl compounds and/or mono- or di-saccharides and/or natural or synthetic invert sugars; and (b) formose which is optionally α-aldolized in the presence of an acid catalyst.
Claim 2
Dependent Claim 86 words
A process for the production of polyether polyols having an average molecular weight of from 200 to 10,000 and an average hydroxyl functionality of from 2.0 to 7.0, comprising reacting one or more cyclic ethers, optionally successively, with a starter comprising: (A) formose which is optionally α-aldolized; or (B) liquid mixtures of: (a) high molecular weight and/or low molecular weight polyhydroxyl compounds and/or mono- or di-saccharides and/or natural or synthetic invert sugars; and (b) formose which is optionally α-aldolized in the presence of an acid catalyst.
Claim 3
Dependent Claim 31 words
The process of claim 1 wherein from 20 to 80% by weight of solutions of crystalline mono- or di-saccharides and/or natural or synthetic invert sugars in formose are used as starter.
Claim 4
Dependent Claim 30 words
The process of claim 2 wherein from 30 to 70% by weight solutions of crystalline mono- or di-saccharides and/or natural or artificial invert sugars in formose are used as starter.
Claim 5
Dependent Claim 51 words
The process of claim 1 wherein the starter contains from 2 to 100% by weight based on the total starter mixture, of dihydric or polyhydric alcohols having a molecular weight of from 62 to 300 and/or polyether, polyester, polyacetal and/or polycarbonate polyols having a molecular weight of from 300 to 4000.
Claim 6
Dependent Claim 18 words
The process of claim 1 wherein formoses having a molecular weight of from 92 to 360 are used.
Claim 7
Dependent Claim 25 words
The process of claim 1 wherein formoses having a content of reducing compounds, expressed as glucose, of from 4 to 85% by weight are used.
Claim 8
Dependent Claim 16 words
The process of claim 1 wherein ethylene oxide and/or propylene oxide are used as cyclic ethers.
Claim 9
Dependent Claim 25 words
The process of claim 1 wherein an adduct of a carboxylic acid or carboxylic acid anhydride with boron trifluoride is used as the acid catalyst.
Claim 10
Dependent Claim 17 words
The process of claim 8, wherein the starter contains from 0.5 to 20% by weight of water.
Claim 11
Dependent Claim 17 words
The process of claim 1 wherein the starter contains from 0.5 to 4% by weight of water.
Claim 12
Dependent Claim 118 words
In a process for the production of optionally cellular polyurethane plastics by reacting: (a) polyisocyanates; with (b) relatively high molecular weight compounds containing isocyanate-reactive hydrogen atoms; and optionally, (c) chain-extenders; optionally in the presence of (d) blowing agents, catalysts and other known additives; the improvement which comprises using the polyether polyols as component (b) which are produced by a process comprising reacting one or more cyclic ethers, optionally successively, with a starter comprising: (A) formose which is optionally α-aldolized; or (B) liquid mixtures of: (a) high molecular weight and/or low molecular weight polyhydroxyl compounds and/or mono- or di-saccharides and/or natural or synthetic invert sugars; and (b) formose which is optionally α-aldolized in the presence of an acid catalyst.
Claim 13
Dependent Claim 118 words
In a process for the production of optionally cellular polyurethane plastics by reacting: (a) polyisocyanates; with (b) relatively high molecular weight compounds containing isocyanate-reactive hydrogen atoms; and optionally, (c) chain-extenders; optionally in the presence of (d) blowing agents, catalysts and other known additives; the improvement which comprises using the polyether polyols as component (b) which are produced by a process comprising reacting one or more cyclic ethers, optionally successively, with a starter comprising: (A) formose which is optionally α-aldolized; or (B) liquid mixtures of: (a) high molecular weight and/or low molecular weight polyhydroxyl compounds and/or mono- or di-saccharides and/or natural or synthetic invert sugars; and (b) formose which is optionally α-aldolized in the presence of an acid catalyst.

References Cited (Backward Citations)

US3202620A Cited
US3846347A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1983-02-04 1983-08-06 1984-02-05 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1987-02-04 1987-08-06 1988-02-05 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1991-02-04 1991-08-06 1992-02-05 $7700.00 Window Closed / Lapsed

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