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US2987524A Expired / Lapsed US ⏱️ 0.0 years remaining

Process for preparing cyclic

Assignee: —
•
Filing: —
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Granted: 1961-06-06
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Expires: 1978-06-06
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Abstract

No abstract record available.

Inventors

No inventors recorded.

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-01 17:00
CPC Classifications
C; C07; C07D; C07D317/00; C07D317/08; C07D317/10; C07D317/12; C07D319/00; C07D319/04; C07D319/06

Claims Analysis

Total Claims: 4
Claim 1
Independent Claim 125 words
A PROCESS FOR PREPARING A CYCLIC UNSATURATED ACETAL COMPRISING REACTING AN ALPHA,BETA-ETHYLENIC MONOALDEHYDE SELECTED FROM THE GROUP OF HYDROCARBON AND CHLORINATED HYDROCARBON MONOALDEHYDES HAVING FROM 3 TO 12 CARBON ATOMS AND WHICH ARE FREE FROM REACTIVE CONSTITUENTS OTHER THAN THE ETHYLENIC DOUBLE BOND, THE CARBONYL GROUP, AND THE CHLORINE ATOM, WITH A POLYOL HAVING TWO CARBINOL GROUPS SEPARATED BY NOT MORE THAN ONE CARBON ATOM, SELECTED FROM THE GROUP CONSISTING OF SATURATED HYDROCARBON AND CHLORINATED HYDROCARBON POLYOLS, IN THE PRESENCE OF 0.02 TO 0.06 MOLE OF A SULFO ACID PER MOLE OF THE MONOALDEHYDE AT A TEMPERATURE OF 60* TO 100*C. FOR NOT MORE THAN THREE HOURS WHILE REMOVING THE WATER FORMED IN THE REACTION, WHEREBY THE CYCLIC ACETAL OF SAID ETHYLENIC ALDEHYDE IS PRODUCED.
Claim 2
Dependent Claim 125 words
A PROCESS FOR PREPARING A CYCLIC UNSATURATED ACETAL COMPRISING REACTING AN ALPHA,BETA-ETHYLENIC MONOALDEHYDE SELECTED FROM THE GROUP OF HYDROCARBON AND CHLORINATED HYDROCARBON MONOALDEHYDES HAVING FROM 3 TO 12 CARBON ATOMS AND WHICH ARE FREE FROM REACTIVE CONSTITUENTS OTHER THAN THE ETHYLENIC DOUBLE BOND, THE CARBONYL GROUP, AND THE CHLORINE ATOM, WITH A POLYOL HAVING TWO CARBINOL GROUPS SEPARATED BY NOT MORE THAN ONE CARBON ATOM, SELECTED FROM THE GROUP CONSISTING OF SATURATED HYDROCARBON AND CHLORINATED HYDROCARBON POLYOLS, IN THE PRESENCE OF 0.02 TO 0.06 MOLE OF A SULFO ACID PER MOLE OF THE MONOALDEHYDE AT A TEMPERATURE OF 60* TO 100*C. FOR NOT MORE THAN THREE HOURS WHILE REMOVING THE WATER FORMED IN THE REACTION, WHEREBY THE CYCLIC ACETAL OF SAID ETHYLENIC ALDEHYDE IS PRODUCED.
Claim 3
Independent Claim 47 words
A METHOD OF PRODUCING 2-VINYL-1,3-DIOXANE WHICH COMPRISES REACTING ACROLEIN WITH 2-METHYL-2,4-PENTANEDIOL AT A TEMPERATURE OF ABOUT 60*-100*C. FOR NOT MORE THAN THREE HOURS IN THE PRESENCE OF 0.02 TO 0.06 MOLE OF A SULFO ACID PER MOLE OF ACROLEIN WHILE REMOVING THE WATER FORMED IN THE REACTION.
Claim 4
Independent Claim 47 words
A METHOD OF PRODUCING 2-VINYL-1,3-DIOXANE WHICH COMPRISES REACTING ACROLEIN WITH 2-METHYL-2,4-PENTANEDIOL AT A TEMPERATURE OF ABOUT 60*-100*C. FOR NOT MORE THAN THREE HOURS IN THE PRESENCE OF 0.02 TO 0.06 MOLE OF A SULFO ACID PER MOLE OF ACROLEIN WHILE REMOVING THE WATER FORMED IN THE REACTION.

References Cited (Backward Citations)

US1934309A Cited
US2131998A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1964-06-05 1964-12-05 1965-06-06 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1968-06-05 1968-12-05 1969-06-06 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1972-06-05 1972-12-05 1973-06-06 $7700.00 Window Closed / Lapsed

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