[go: up one dir, main page]

Madadi, 2021 - Google Patents

Strecker Synthesis of a-aminonitriles Facilitated by N-methyl Imidazolium Acetate.

Madadi, 2021

Document ID
12762666061296538993
Author
Madadi E
Publication year
Publication venue
Alinteri Journal of Agriculture Sciences

External Links

Snippet

N-Methyl imidazolium acetate [HMIm] OAc was simply prepared through reaction of N- methyl imidazole with acetic acid and it was applied as a media and promoter for Strecker synthesis of α-aminonitriles. The three component reaction of a variety of structurally …
Continue reading at search.ebscohost.com (other versions)

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C253/00Preparation of carboxylic acid nitriles
    • C07C253/30Preparation of carboxylic acid nitriles by reactions not involving the formation of cyano groups
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2101/00Systems containing only non-condensed rings
    • C07C2101/12Systems containing only non-condensed rings with a six-membered ring
    • C07C2101/14The ring being saturated
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C231/00Preparation of carboxylic acid amides
    • C07C231/02Preparation of carboxylic acid amides from carboxylic acids or from esters, anhydrides, or halides thereof by reaction with ammonia or amines
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C231/00Preparation of carboxylic acid amides
    • C07C231/06Preparation of carboxylic acid amides from nitriles by transformation of cyano groups into carboxamide groups
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C233/00Carboxylic acid amides
    • C07C233/01Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms
    • C07C233/02Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having nitrogen atoms of carboxamide groups bound to hydrogen atoms or to carbon atoms of unsubstituted hydrocarbon radicals
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C231/00Preparation of carboxylic acid amides
    • C07C231/08Preparation of carboxylic acid amides from amides by reaction at nitrogen atoms of carboxamide groups
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C209/00Preparation of compounds containing amino groups bound to a carbon skeleton
    • C07C209/44Preparation of compounds containing amino groups bound to a carbon skeleton by reduction of carboxylic acids or esters thereof in presence of ammonia or amines, or by reduction of nitriles, carboxylic acid amides, imines or imino-ethers
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C231/00Preparation of carboxylic acid amides
    • C07C231/12Preparation of carboxylic acid amides by reactions not involving the formation of carboxamide groups
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C253/00Preparation of carboxylic acid nitriles
    • C07C253/20Preparation of carboxylic acid nitriles by dehydration of carboxylic acid amides
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C227/00Preparation of compounds containing amino and carboxyl groups bound to the same carbon skeleton
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C201/00Preparation of esters of nitric or nitrous acid or of compounds containing nitro or nitroso groups bound to a carbon skeleton
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C51/00Preparation of carboxylic acids or their salts, halides or anhydrides
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C277/00Preparation of guanidine or its derivatives, i.e. compounds containing the group, the singly-bound nitrogen atoms not being part of nitro or nitroso groups
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C229/00Compounds containing amino and carboxyl groups bound to the same carbon skeleton
    • C07C229/02Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C255/00Carboxylic acid nitriles
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07BGENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B2200/00Indexing scheme relating to specific properties of organic compounds
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS

Similar Documents

Publication Publication Date Title
Takemoto Recognition and activation by ureas and thioureas: stereoselective reactions using ureas and thioureas as hydrogen-bonding donors
Handa et al. Heterobimetallic transition metal/rare earth metal bifunctional catalysis: a Cu/Sm/Schiff base complex for syn-selective catalytic asymmetric nitro-Mannich reaction
Pellissier Recent developments in asymmetric aziridination
Brindle et al. Chiral β-iodoamines by urea-catalysed iodocyclization of trichloroacetimidates
Chhatwal et al. Direct synthesis of amides from nonactivated carboxylic acids using urea as nitrogen source and Mg (NO 3) 2 or imidazole as catalysts
Muniyappa et al. A simple and greener approach for the amide bond formation employing FeCl 3 as a catalyst
US20070161813A1 (en) Process for preparing nitriles and isonitriles by dehydration reactions with propanephosphonic anhydrides
Ying et al. Green and efficient aza-Michael additions of aromatic amines to α, β-unsaturated ketones catalyzed by DBU based task-specific ionic liquids without solvent
CN110088085B (en) Method for producing methionine
Hajzer et al. Enantioselective Michael addition of the 2‐(1‐ethylpropoxy) acetaldehyde to N‐[(1Z)‐2‐nitroethenyl] acetamide–optimization of the key step in the organocatalytic oseltamivir synthesis
RU2600741C2 (en) Methods of producing 1,5,7-triazabicycl[4,4,0]-dec-5-ene from reaction of disubstituted carbodiimide and dipropylene triamine
Madadi Strecker Synthesis of a-aminonitriles Facilitated by N-methyl Imidazolium Acetate.
Madadi Strecker synthesis of α-aminonitriles facilitated by N-methyl imidazolium acetate.
JP5155666B2 (en) Process for the synthesis of glycolonitrile
JP3762980B2 (en) Amino group introduction method and amino acid synthesis method
JP6748634B2 (en) Method for producing primary amine by continuous catalytic reduction of nitriles
US9994720B2 (en) Methods for producing 1,5,7-triazabicyclo[4.4.0]dec-5-ene by reaction of a disubstituted carbodiimide and dipropylene triamine
Li et al. Cyanoaroylation of imines bearing a thiazole ring using potassium hexacyanoferrate (II) as an eco-friendly cyanide source
MXPA05004158A (en) Process for the production of 3-methylthiopropanal.
Akbari et al. Guanidine derived ionic liquids: catalyst free medium for N-Formylation of amines
Tagliapietra et al. Green enabling technologies for competitive synthesis of pharmaceutical lead compounds
Muratov et al. Formal reductive addition of acetonitrile to aldehydes and ketones
Yaragorla et al. Tris (pentafluorophenyl) borane catalyzed synthesis of cyanohydrins, cyanohydrin trimethylsilyl ethers and alpha-amino nitriles
CN105669485B (en) A kind of preparation method of amide compound
CN103304443B (en) Method for catalyzing and condensing aromatic aldehyde and active methylene compound by using multi-amino ionic liquid