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Extract from the Register of European Patents

EP About this file: EP2809637

EP2809637 - PROCESS FOR PRODUCING DODECANE-1, 12-DIOL BY REDUCTION OF LAURYL LACTONE PRODUCED FROM THE OXIDATION OF CYCLODODECANONE [Right-click to bookmark this link]
StatusThe application is deemed to be withdrawn
Status updated on  24.06.2016
Database last updated on 06.07.2024
Most recent event   Tooltip24.06.2016Application deemed to be withdrawnpublished on 27.07.2016  [2016/30]
Applicant(s)For all designated states
Invista Technologies S.A R.L.
Zweigniederlassung St. Gallen
Kreuzackerstrasse 9
9000 St. Gallen / CH
[2014/50]
Inventor(s)01 / HASTINGS, James D.
401 Charleston Drive
Victoria, TX 77904-3816 / US
02 / HERKES, Frank E.
223 Charleston Drive
Wilmington, DE 19808-4358 / US
03 / RAJENDRAN, Gurusamy
1892 Lake Landing Drive
League City, TX 77573 / US
04 / SUN, Qun
154 New Granville Road
Wilmington, DE 19808-1106 / US
 [2014/50]
Representative(s)Cockerton, Bruce Roger
Carpmaels & Ransford LLP
One Southampton Row
London WC1B 5HA / GB
[2014/50]
Application number, filing date13703211.621.01.2013
WO2013US22408
Priority number, dateUS201261593452P01.02.2012         Original published format: US 201261593452 P
[2014/50]
Filing languageEN
Procedural languageEN
PublicationType: A1 Application with search report
No.:WO2013116029
Date:08.08.2013
Language:EN
[2013/32]
Type: A1 Application with search report 
No.:EP2809637
Date:10.12.2014
Language:EN
The application published by WIPO in one of the EPO official languages on 08.08.2013 takes the place of the publication of the European patent application.
[2014/50]
Search report(s)International search report - published on:EP08.08.2013
ClassificationIPC:C07C29/149, C07D313/00, C07C31/20
[2014/50]
CPC:
C07C29/149 (EP,CN,US); C07C29/147 (US); C07D313/00 (EP,CN,US)
C-Set:
C07C29/149, C07C31/20 (CN,EP,US);
C07C29/149, C07C31/207 (CN)
Designated contracting statesAL,   AT,   BE,   BG,   CH,   CY,   CZ,   DE,   DK,   EE,   ES,   FI,   FR,   GB,   GR,   HR,   HU,   IE,   IS,   IT,   LI,   LT,   LU,   LV,   MC,   MK,   MT,   NL,   NO,   PL,   PT,   RO,   RS,   SE,   SI,   SK,   SM,   TR [2014/50]
TitleGerman:VERFAHREN ZUR HERSTELLUNG VON DODECAN-1,12-DIOL DURCH REDUZIERUNG DES DURCH DIE OXIDIERUNG VON CYCLODODECANON PRODUZIERTEN LAURYL-LACTONS[2014/50]
English:PROCESS FOR PRODUCING DODECANE-1, 12-DIOL BY REDUCTION OF LAURYL LACTONE PRODUCED FROM THE OXIDATION OF CYCLODODECANONE[2014/50]
French:PROCÉDÉ DE PRODUCTION DE DODÉCANE-1,12-DIOL PAR RÉDUCTION DE LAURYL LACTONE PRODUIT À PARTIR DE L'OXYDATION DE LA CYCLODODÉCANONE[2014/50]
Entry into regional phase05.08.2014National basic fee paid 
05.08.2014Designation fee(s) paid 
05.08.2014Examination fee paid 
Examination procedure02.12.2013Request for preliminary examination filed
International Preliminary Examining Authority: EP
05.08.2014Examination requested  [2014/50]
23.01.2015Amendment by applicant (claims and/or description)
15.09.2015Despatch of a communication from the examining division (Time limit: M04)
26.01.2016Application deemed to be withdrawn, date of legal effect  [2016/30]
23.02.2016Despatch of communication that the application is deemed to be withdrawn, reason: reply to the communication from the examining division not received in time  [2016/30]
Divisional application(s)The date of the Examining Division's first communication in respect of the earliest application for which a communication has been issued is  15.09.2015
Fees paidRenewal fee
13.01.2015Renewal fee patent year 03
Penalty fee
Additional fee for renewal fee
31.01.201604   M06   Not yet paid
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Cited inInternational search[Y]EP1566372  (NEW JAPAN CHEM CO LTD [JP]) [Y] 18-32 * paragraph [0042] - paragraph [0043] *;
 [XY]  - KENNETH B. WIBERG ET AL, "Lactones. 2. Enthalpies of hydrolysis, reduction, and formation of the C4-C13 monocyclic lactones. Strain energies and conformations", JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, (19910901), vol. 113, no. 20, doi:10.1021/ja00020a036, ISSN 0002-7863, pages 7697 - 7705, XP055042021 [X] 1-3,8 * page 7699, table IV, entry 9 * * page 7699, column 2, line 5 - line 16 * * page 7703, table XII, entry 6 * * page 7703, column 1, paragraph 3 * [Y] 4-7,9-32

DOI:   http://dx.doi.org/10.1021/ja00020a036
 [Y]  - BIDD I ET AL, "CONVENIENT SYNTHESES OF BIFUNCTIONAL C12-ACYCLIC COMPOUNDS FROM CYCLODODECANONE", JOURNAL OF THE CHEMICAL SOCIETY, PERKIN TRANSACTIONS 1, CHEMICAL SOCIETY, LETCHWORTH; GB, (19830101), no. 7, doi:10.1039/P19830001369, ISSN 0300-922X, pages 1369 - 1372, XP002043408 [Y] 4-7,9-17 * page 1370, column 2, paragraph 4 - page 1371, column 1, paragraph 1 *

DOI:   http://dx.doi.org/10.1039/p19830001369
 [A]  - JEAN PIERRE GENET ET AL, "A new synthesis of 14-tetradecanolide from cyclododecanone.", TETRAHEDRON LETTERS, (19800101), vol. 21, no. 16, doi:10.1016/S0040-4039(00)92763-1, ISSN 0040-4039, pages 1521 - 1524, XP055042065 [A] 1,30-32 * scheme I *

DOI:   http://dx.doi.org/10.1016/S0040-4039(00)92763-1
by applicant   - IAN T. HARRISON; SHUYEN HARRISON, Compendium of Organic Synthetic Methods, JOHN WILEY & SONS, (1971), vol. 1
    - IAN T. HARRISON; SHUYEN HARRISON, COMPENDIUM OF ORGANIC SYNTHETIC METHODS, (1974), vol. 2
    - LOUIS S. HEGEDUS; LEROY WADE, COMPENDIUM OF ORGANIC SYNTHETIC METHODS, (1977), vol. 3
    - LEROY G. WADE JR., COMPENDIUM OF ORGANIC SYNTHETIC METHODS, (1980), vol. 4
    - LEROY G. WADE JR., COMPENDIUM OF ORGANIC SYNTHETIC METHODS, (1984), vol. 5
    - MICHAEL B. SMITH, COMPENDIUM OF ORGANIC SYNTHETIC METHODS, vol. 6
    - Comprehensive Organic Synthesis. Selectivity, Strategy & Efficiency in Modem Organic Chemistry, PERGAMON PRESS, (1993), vol. 9
    - IAN T. HARRISON; SHUYEN HARRISON, Compendium of Organic Synthetic Methods, (1974), vol. 2
    - LEROY G.; WADE JR., COMPENDIUM OF ORGANIC SYNTHETIC METHODS, (1980), vol. 4
    - LEROY G.; WADE JR., COMPENDIUM OF ORGANIC SYNTHETIC METHODS, (1984), vol. 5
The EPO accepts no responsibility for the accuracy of data originating from other authorities; in particular, it does not guarantee that it is complete, up to date or fit for specific purposes.