ES336677A1 - Preparation of cyclododecanone oxime - Google Patents

Preparation of cyclododecanone oxime

Info

Publication number
ES336677A1
ES336677A1 ES336677A ES336677A ES336677A1 ES 336677 A1 ES336677 A1 ES 336677A1 ES 336677 A ES336677 A ES 336677A ES 336677 A ES336677 A ES 336677A ES 336677 A1 ES336677 A1 ES 336677A1
Authority
ES
Spain
Prior art keywords
oxime
cyclododecanone
solvent
cyclododecanone oxime
range
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
ES336677A
Other languages
Spanish (es)
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Stamicarbon BV
Original Assignee
Stamicarbon BV
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Stamicarbon BV filed Critical Stamicarbon BV
Publication of ES336677A1 publication Critical patent/ES336677A1/en
Expired legal-status Critical Current

Links

Abstract

Cyclododecanone oxime is prepared by reacting cyclododecanone at 15-120 C. in the presence of a water-miscible solvent with an aqueous solution of a hydroxylamine mineral acid salt, the pH being kept in the range of from 4-6 by addition of a base and the said watermiscible solvent being an organic solvent with a boiling point in the range from 60 to 120 C., whereby two heterogeneous liquid organic and aqueous phases are formed and cyclododecanone oxime is obtained from the organic phase. Specified solvents are dioxane, propanol, isopropanol, tertiary butanol, acetonitrile and tetrahydrofuran. In a modification, a waterimmiscible extraction liquid in which the oxime dissolves is added before the two heterogeneous phases are separated.
ES336677A 1966-02-11 1967-02-10 Preparation of cyclododecanone oxime Expired ES336677A1 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
NL6601799A NL146488B (en) 1966-02-11 1966-02-11 PREPARING CYCLODODECANONOXIME.

Publications (1)

Publication Number Publication Date
ES336677A1 true ES336677A1 (en) 1968-01-16

Family

ID=19795713

Family Applications (1)

Application Number Title Priority Date Filing Date
ES336677A Expired ES336677A1 (en) 1966-02-11 1967-02-10 Preparation of cyclododecanone oxime

Country Status (7)

Country Link
BE (1) BE693901A (en)
CH (1) CH477414A (en)
DE (1) DE1263761B (en)
ES (1) ES336677A1 (en)
FR (1) FR1516286A (en)
GB (1) GB1148013A (en)
NL (1) NL146488B (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2008096873A1 (en) 2007-02-09 2008-08-14 National University Corporation Nagoya University Method for production of laurolactam
ES2513826T3 (en) * 2007-11-29 2014-10-27 Ube Industries, Ltd. Method for the production of laurolactam

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1081884B (en) * 1959-02-13 1960-05-19 Basf Ag Process for the preparation of cyclododecanone oxime
GB972107A (en) * 1962-09-01 1964-10-07 Basf Ag Production of oximes of cycloaliphatic ketones

Also Published As

Publication number Publication date
DE1263761B (en) 1968-03-21
BE693901A (en) 1967-08-10
NL6601799A (en) 1967-08-14
NL146488B (en) 1975-07-15
GB1148013A (en) 1969-04-10
FR1516286A (en) 1968-03-08
CH477414A (en) 1969-08-31

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