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US3920573A Expired / Lapsed US ⏱️ 0.0 years remaining

Preparation of mixtures of bisphenol A and F

Assignee: Shell USA Inc
•
Filing: 1973-09-28
•
Granted: 1975-11-18
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Expires: 1993-09-28
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Abstract

Abstract Mixtures containing a major proportion of 2,2-bis(4hydroxyphenyl)propane and a minor proportion, e.g. 10-30 percent w, of the isomers of bis(hydroxyphenyl)methane are prepared by allowing a phenolic compound to react with mixtures of acetone and formaldehyde (preferably as trioxane). The recovered mixture of bisphenols serves as the starting material for the production of low viscosity epoxy resins.

Inventors

  • 👤 Geert C Vegter
  • 👤 Gogh Johan Van

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-04 12:09
CPC Classifications
C; C07; C07D; C07D303/00; C07D303/02; C07D303/12; C07D303/18; C07D303/20; C07D303/24; C07C; C07C37/00; C07C37/11; C07C37/20; C08; C08G; C08G59/00; C08G59/18; C08G59/20; C08G59/22; C08G59/24; C08G59/245

Claims Analysis

Total Claims: 7
Claim 1
Independent Claim 136 words
THE PROCESS FOR PREPARING A MIXTURE OF DIPHENYLOALKANES CONSISTING ESSENTIALLY OF CONTACTING A PHENOLIC COMPOUND OR COMPOUNDS, WITH A MIXTURE OF ACETONE AND FORMALDEHYDE OR A PRECURSOR OF FORMALDEHYDE IN THE PRESENCE OF AN ACID CATALYST AND OPTONALLY A BETA-MERCAPTOR PROPANOIC OR THIOL CO-CATALYST, WHERE; I. THE MOLAR RATIO OF ACETONE TO FORMALDEHYDE IS FROM ABOUT 20:1 TO ABOUT 0.5:1, II. THE MOLAR RATIO OF PHENOLIC COMPOUND OR COMPOUNDS TO THE SUM OF THE ACETONE AND FORMALDEHYDE IS FROM ABOUT 10:1 TO ABOUT 25:1, III. THE REACTION TEMPERATURE IS FROM ABOUT 20*C TO ABOUT 110*C, IV. THE REACTION TIME IS FROM ABOUT 0.25 HR. TO ABOUT 5 HR. AND RECOVERING THE RESULTING MIXTURE OF DIPHENYLOLPROPANE AND DIPHENYLOLMETHANE HAVING LESS THAN 10 PERCENT BY WEIGHT OF BY-PRODUCTS IN WHICH A MOLECULE CONTAINS MORE THAN 2 PHENOLIC GROUPS.
Claim 2
Dependent Claim 136 words
THE PROCESS FOR PREPARING A MIXTURE OF DIPHENYLOALKANES CONSISTING ESSENTIALLY OF CONTACTING A PHENOLIC COMPOUND OR COMPOUNDS, WITH A MIXTURE OF ACETONE AND FORMALDEHYDE OR A PRECURSOR OF FORMALDEHYDE IN THE PRESENCE OF AN ACID CATALYST AND OPTONALLY A BETA-MERCAPTOR PROPANOIC OR THIOL CO-CATALYST, WHERE; I. THE MOLAR RATIO OF ACETONE TO FORMALDEHYDE IS FROM ABOUT 20:1 TO ABOUT 0.5:1, II. THE MOLAR RATIO OF PHENOLIC COMPOUND OR COMPOUNDS TO THE SUM OF THE ACETONE AND FORMALDEHYDE IS FROM ABOUT 10:1 TO ABOUT 25:1, III. THE REACTION TEMPERATURE IS FROM ABOUT 20*C TO ABOUT 110*C, IV. THE REACTION TIME IS FROM ABOUT 0.25 HR. TO ABOUT 5 HR. AND RECOVERING THE RESULTING MIXTURE OF DIPHENYLOLPROPANE AND DIPHENYLOLMETHANE HAVING LESS THAN 10 PERCENT BY WEIGHT OF BY-PRODUCTS IN WHICH A MOLECULE CONTAINS MORE THAN 2 PHENOLIC GROUPS.
Claim 3
Dependent Claim 13 words
The process of claim 1 in which the phenolic compound is phenol itself.
Claim 4
Dependent Claim 19 words
The process of claim 2 where the acetone to formaldehyde molar ratio is from about 5:1 to about 1:1.
Claim 5
Dependent Claim 21 words
The process of claim 3 where the phenol to acetone plus formaldehyde mole ratio is from about 14:1 to about 16:1.
Claim 6
Dependent Claim 16 words
The process of claim 4 where the reaction time is from 0.5 hr. to 1 hr.
Claim 7
Dependent Claim 15 words
The process of claim 5 where the formaldehyde is added as the formaldehyde precursor, trioxane.

References Cited (Backward Citations)

US2792429A Cited
US3075015A Cited
US3418378A Cited
US3627846A Cited
US3673262A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1978-11-17 1979-05-19 1979-11-18 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1982-11-17 1983-05-19 1983-11-18 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1986-11-17 1987-05-19 1987-11-18 $7700.00 Window Closed / Lapsed

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