GB809410A - Improved method for the preparation of n-methyleneglycino-nitrile - Google Patents

Improved method for the preparation of n-methyleneglycino-nitrile

Info

Publication number
GB809410A
GB809410A GB3634257A GB3634257A GB809410A GB 809410 A GB809410 A GB 809410A GB 3634257 A GB3634257 A GB 3634257A GB 3634257 A GB3634257 A GB 3634257A GB 809410 A GB809410 A GB 809410A
Authority
GB
United Kingdom
Prior art keywords
cyanide
mols
mol
formaldehyde
excess
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
GB3634257A
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.)
Individual
Original Assignee
Individual
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 Individual filed Critical Individual
Priority to GB3634257A priority Critical patent/GB809410A/en
Publication of GB809410A publication Critical patent/GB809410A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C255/00Carboxylic acid nitriles

Abstract

N-methyleneglycinonitrile is prepared by simultaneously adding substantially 2 mols. of formaldehyde and substantially 1 mol. of an alkali metal cyanide to an excess proportionate quantity of from more than 1 to substantially 2 mols. of an ammonium halide in aqueous solution at a temperature of from - 20 DEG to 10 DEG C., preferably 0-10 DEG C., while maintaining the reaction mass at a pH below 6, and subsequently recovering N-methyleneglycinonitrile. Preferably the acidity is maintained by the addition, towards the termination of the reaction, of a water-soluble non-reactive carboxylic acid, such as acetic acid in amount at least 0.05 mol. per cent based on the alkali metal cyanide. The preferred proportionate quantity of ammonium halide is substantially 1.4 mols. Preferably the formaldehyde and cyanide are continuously added so as to provide a slight excess of formaldehyde over its required 2 : 1 molar ratio with respect to the cyanide, e.g. at least a 5 mol. per cent excess. Preferred reactants are sodium cyanide and ammonium chloride. The product normally precipitates as a crystalline substance and may be separated by filtration, decantation, or the like.
GB3634257A 1957-11-21 1957-11-21 Improved method for the preparation of n-methyleneglycino-nitrile Expired GB809410A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB3634257A GB809410A (en) 1957-11-21 1957-11-21 Improved method for the preparation of n-methyleneglycino-nitrile

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB3634257A GB809410A (en) 1957-11-21 1957-11-21 Improved method for the preparation of n-methyleneglycino-nitrile

Publications (1)

Publication Number Publication Date
GB809410A true GB809410A (en) 1959-02-25

Family

ID=10387270

Family Applications (1)

Application Number Title Priority Date Filing Date
GB3634257A Expired GB809410A (en) 1957-11-21 1957-11-21 Improved method for the preparation of n-methyleneglycino-nitrile

Country Status (1)

Country Link
GB (1) GB809410A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0280174A2 (en) * 1987-02-20 1988-08-31 Hitachi, Ltd. Compounds having schiff bonds, polymers thereof,and process for preparing the same
US6496831B1 (en) * 1999-03-25 2002-12-17 Lucent Technologies Inc. Real-time event processing system for telecommunications and other applications
US6681230B1 (en) * 1999-03-25 2004-01-20 Lucent Technologies Inc. Real-time event processing system with service authoring environment

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0280174A2 (en) * 1987-02-20 1988-08-31 Hitachi, Ltd. Compounds having schiff bonds, polymers thereof,and process for preparing the same
EP0280174A3 (en) * 1987-02-20 1988-11-30 Hitachi, Ltd. Compounds having schiff bonds, polymers thereof,and process for preparing the same
US4900807A (en) * 1987-02-20 1990-02-13 Hitachi, Ltd. Polymer from nitrile terminated compounds having Schiff bonds and process for preparing the same
US6496831B1 (en) * 1999-03-25 2002-12-17 Lucent Technologies Inc. Real-time event processing system for telecommunications and other applications
US6681230B1 (en) * 1999-03-25 2004-01-20 Lucent Technologies Inc. Real-time event processing system with service authoring environment

Similar Documents

Publication Publication Date Title
GB809410A (en) Improved method for the preparation of n-methyleneglycino-nitrile
GB1138883A (en) A method for preparing an -‡-aminoaliphaticcarboxylic acid from the corresponding -‡-chlorocarboxylic acid and ammonia
US2692281A (en) Preparation of hydrazodicarbonamide
GB1167679A (en) Production of 2-Hydroxy-4-Alkoxybenzophenones
GB805021A (en) Process for n, n-diisopropylbenzo-thiazole-2-sulfenamide
GB803179A (en) Process for the preparation of hypophosphites
ES252067A1 (en) Preparation of azacyclo-2, 3-alkene-2-chloro-n-carbochloride
US2823222A (en) Method for the preparation of n-methylene-glycinonitrile
GB1298279A (en) Process for the preparation of alpha glucoheptonate dihydrate
IE36829B1 (en) Process for the preparation of penicillamine
GB1006352A (en) Production of salts or sorbic acid
GB871380A (en) Method of preparing tetraalkali metal salts of ethylenediaminetetraacetic acid
GB990757A (en) Process for the preparation of 3-acetamido-5-amino-2,4,6,-triiodobenzoic acid
GB1257270A (en)
GB1157393A (en) Process for the Preparation of Aminoacetic Acid
GB956075A (en) Improvements in or relating to the production of alkali metal fluoborates
GB1505610A (en) Process for preparing 3,4-dicyano-1,2,5-thiadiazole
ES253183A1 (en) Magnesium glutamate hydrobromide and processes for the production thereof
GB1260072A (en) Process for the production of 2-hydroxyquinoline-4-carboxylic acids and salts thereof
GB1124149A (en) Process for the preparation of ª‡-amino acids
GB837467A (en) Salts of thiodiglycolic acid and their preparation
GB1301197A (en) A method of preparing amine salts of 2.4-dichlorophenoxyacetic acid
GB887691A (en) Aromatic fluorine compounds employed in the production of polymeric gums
GB1419335A (en) Process for the production of 1,1,2-triacetoxy ethane
GB1089825A (en) Process for obtaining amino-guanidine bicarbonate