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2,10 - dioxa - 5 - aza-tricyclo(6,2,1,0**1,5) undecanedion-(6,9) and 2,11-dioxa-6-aza -tricyclo(7,2,1,0**1,6)dodecandedion-(7,10) compounds and their preparation

Assignee: Huels AG
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Filing: 1968-09-20
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Granted: 1971-03-30
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Expires: 1988-09-20
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Abstract

Abstract SUBSTITUTED $2-OXAZOLINES AND 4H-5,6-DIHYDRO-1,3-OXAZINES ARE CONVERTED INTO LACTONES CONTAINING AMIDE GROUPS BY REACTING WITH MALEIC ACID ANHYDRIDE, UNDER EXCLUSION OF MOISTURE AND AT A TEMPERATURE OF 0-180*C., FROM 0.2 TO 1.0 MOLE OF THE MALEIC ACID ANHYDRIDE BEING EMPLOYED PER MOL OF THE OXAZOLINE OR OXAZINE. THE LACTONE PRODUCTS ARE UTILIZABLE AS INHIBITORS OF PLANT GROWTH; ALSO, AS SYNTHETIC COMPONENTS OF DRUGS.

Inventors

  • 👤 Rudolf Nehring

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-25 11:38
CPC Classifications
C; C07; C07D; C07D498/00; C07D498/12; C07D498/18

Claims Analysis

Total Claims: 0
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References Cited (Backward Citations)

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USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1974-03-29 1974-09-28 1975-03-30 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1978-03-29 1978-09-28 1979-03-30 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1982-03-29 1982-09-28 1983-03-30 $7700.00 Window Closed / Lapsed

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