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GB939682A - Substituted malonic acid dinitriles - Google Patents

Substituted malonic acid dinitriles

Info

Publication number
GB939682A
GB939682A GB3821861A GB3821861A GB939682A GB 939682 A GB939682 A GB 939682A GB 3821861 A GB3821861 A GB 3821861A GB 3821861 A GB3821861 A GB 3821861A GB 939682 A GB939682 A GB 939682A
Authority
GB
United Kingdom
Prior art keywords
prepared
formamidinium
substituted
acid
oxapentamethylene
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
GB3821861A
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.)
Bayer AG
Original Assignee
Bayer AG
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 Bayer AG filed Critical Bayer AG
Publication of GB939682A publication Critical patent/GB939682A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D295/00Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
    • C07D295/16Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms
    • C07D295/18Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms by radicals derived from carboxylic acids, or sulfur or nitrogen analogues thereof
    • C07D295/195Radicals derived from nitrogen analogues of carboxylic acids
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C255/00Carboxylic acid nitriles
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D295/00Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
    • C07D295/02Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms containing only hydrogen and carbon atoms in addition to the ring hetero elements

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)

Abstract

N-substituted aminomalonic acid dinitriles are prepared by reacting 1 mol. of an N,N,N1,N1- tetrasubstituted formamidinium salt with at least 2 mols. of anhydrous hydrocyanic acid. Preferred N,N,N1,N1-tetra-substituted formamidinium salts have the formula:- <FORM:0939682/IV(a)/1> in which R and R1 separately represents aliphatic, cycloaliphatic or aromatic radicals which may be substituted by alkyl or alkoxy groups, chlorine or bromine or in which a group R together with an adjacent group R1 represent a C4-5 alkylene bridge in which one methylene group can be replaced by O, N or S, and X represents an anion such as that derived from hydrochloric, hydrobromic, hydroiodic, chloric, iodic, perchloric or sulphuric acid. The process yields amine salts as by-products. p N,N,N1,N1- Bis- (pentamethylene)- formamidinium chloride is prepared by heating excess of tetramethyl formamidinium chloride with excess piperidine. N,N,N1,N1- Bis- (3- oxapentamethylene)-formamidinium chloride is prepared by reacting N-formyl morpholine with chloroformic acid-3-oxapentamethylene amide. Chloroformic acid- 3- oxapentamethylene amide is prepared by reacting N-methyl morpholine with phosgene in boiling benzene.
GB3821861A 1960-11-16 1961-10-25 Substituted malonic acid dinitriles Expired GB939682A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DEF32561A DE1128431B (en) 1960-11-16 1960-11-16 Process for the preparation of basic substituted malonic dinitriles

Publications (1)

Publication Number Publication Date
GB939682A true GB939682A (en) 1963-10-16

Family

ID=7094685

Family Applications (1)

Application Number Title Priority Date Filing Date
GB3821861A Expired GB939682A (en) 1960-11-16 1961-10-25 Substituted malonic acid dinitriles

Country Status (4)

Country Link
BE (1) BE610352A (en)
CH (1) CH396934A (en)
DE (1) DE1128431B (en)
GB (1) GB939682A (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN105985263B (en) * 2015-02-03 2019-02-15 兰州大学 A kind of synthetic method of N,N-disubstituted amino-malononitrile compounds

Also Published As

Publication number Publication date
BE610352A (en) 1962-03-16
CH396934A (en) 1965-08-15
DE1128431B (en) 1962-04-26

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