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Extract from the Register of European Patents

EP About this file: EP0296517

EP0296517 - Process for preparing monohalogenated benzocyclobutene [Right-click to bookmark this link]
Former [1988/52]Process for preparing monohalogenated cyclobutarenes
[1993/30]
StatusNo opposition filed within time limit
Status updated on  02.06.1994
Database last updated on 05.10.2024
Most recent event   Tooltip26.04.2002Lapse of the patent in a contracting state
New state(s): ES
published on 12.06.2002  [2002/24]
Applicant(s)For all designated states
The Dow Chemical Company
2020 Dow Center
Midland, Michigan 48674 / US
[N/P]
Former [1988/52]For all designated states
THE DOW CHEMICAL COMPANY
2030 Dow Center Abbott Road P.O. Box 1967
Midland Michigan 48640-1967 / US
Inventor(s)01 / Liu, Ming-Biann
386 Mt. Sequoia Place
Clayton California 94517 / US
[1988/52]
Representative(s)Sternagel, Hans-Günther, et al
Patentanwälte Sternagel & Fleischer Braunsberger Feld 29
51429 Bergisch Gladbach / DE
[N/P]
Former [1988/52]Sternagel, Hans-Günther, Dr., et al
Patentanwälte Dr. Michael Hann Dr. H.-G. Sternagel Sander Aue 30
D-51465 Bergisch Gladbach / DE
Application number, filing date88109765.318.06.1988
[1988/52]
Priority number, dateUS1987006471422.06.1987         Original published format: US 64714
[1988/52]
Filing languageEN
Procedural languageEN
PublicationType: A2 Application without search report 
No.:EP0296517
Date:28.12.1988
Language:EN
[1988/52]
Type: A3 Search report 
No.:EP0296517
Date:18.10.1989
Language:EN
[1989/42]
Type: B1 Patent specification 
No.:EP0296517
Date:28.07.1993
Language:EN
[1993/30]
Search report(s)(Supplementary) European search report - dispatched on:EP31.08.1989
ClassificationIPC:C07C25/18, C07C17/12
[1988/52]
CPC:
C07C17/12 (EP,US); C07C25/22 (KR)
C-Set:
C07C17/12, C07C25/18 (EP,US)
Designated contracting statesAT,   BE,   CH,   DE,   ES,   FR,   GB,   IT,   LI,   NL,   SE [1988/52]
TitleGerman:Verfahren zur Herstellung von monohalogeniertem Benzocyclobuten[1993/30]
English:Process for preparing monohalogenated benzocyclobutene[1993/30]
French:Procédé pour la fabrication de benzocyclobutène monohalogené[1993/30]
Former [1988/52]Verfahren zur Herstellung von monobromierten Cyclobutarenen
Former [1988/52]Process for preparing monohalogenated cyclobutarenes
Former [1988/52]Procédé pour la fabrication de cyclo-butarènes monobrominés
Examination procedure09.04.1990Examination requested  [1990/23]
06.11.1991Despatch of a communication from the examining division (Time limit: M06)
06.05.1992Reply to a communication from the examining division
23.09.1992Despatch of communication of intention to grant (Approval: Yes)
21.01.1993Communication of intention to grant the patent
08.04.1993Fee for grant paid
08.04.1993Fee for publishing/printing paid
Opposition(s)29.04.1994No opposition filed within time limit [1994/29]
Fees paidRenewal fee
07.03.1990Renewal fee patent year 03
15.03.1991Renewal fee patent year 04
02.03.1992Renewal fee patent year 05
26.02.1993Renewal fee patent year 06
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Responsibility for the accuracy, completeness or quality of the data displayed under the link provided lies entirely with the Unified Patent Court.
Lapses during opposition  TooltipAT28.07.1993
ES28.07.1993
[2002/24]
Former [1994/19]AT28.07.1993
Documents cited:Search[XD]US4540763  (KIRCHHOFF ROBERT A [US]);
 [X]WO8701383  (DOW CHEMICAL CO [US])
 [XD]  - TETRAHEDRON
 [X]  - JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
    [ ] - JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Examination   - TETRAHEDRON, vol. 21, 1965, pages 245-254, London, GB; J. B. F. LLOYD et al, "The electrophilic substitution of benzocyclobutene-II"
    - JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, vol. 80, no. 9, 9 May 1958, pages 2255-2257, Columbus, Ohio, USA; M. P. CAVA et al, "Condensed cyclobutane aromatic systems. IV. Benzocyclobutene and 1-bromobenzocyclobutene"
    - JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, vol. 99, no. 12, 8 June 1977, pages 4058-4069, Columbus, Ohio, USA; R. L. HILLARD III et al, "Substituted benzocyclobutenes, indans and tetralins via cobalt-catalyzed cooligomerization of alpha,omega-diynes with substituted acetylenes. Formation and synthetic utility of trimethylsilylated benzocycloalkenes"
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