GB851783A - Production of nitrilotriacetonitrile - Google Patents

Production of nitrilotriacetonitrile

Info

Publication number
GB851783A
GB851783A GB6367/59A GB636759A GB851783A GB 851783 A GB851783 A GB 851783A GB 6367/59 A GB6367/59 A GB 6367/59A GB 636759 A GB636759 A GB 636759A GB 851783 A GB851783 A GB 851783A
Authority
GB
United Kingdom
Prior art keywords
prepared
acids
concentrated
solution
reacting
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
GB6367/59A
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.)
Roehm and Haas GmbH
Original Assignee
Roehm and Haas GmbH
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 Roehm and Haas GmbH filed Critical Roehm and Haas GmbH
Publication of GB851783A publication Critical patent/GB851783A/en
Expired legal-status Critical Current

Links

Classifications

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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)

Abstract

Nitrilotriacetonitrile is prepared by reacting hydrocyanic acid and formaldehyde with one or more compounds of formula HO3S.NRR1, where R and R1 which may be the same or different, are H or -SO3H, e.g. by adding formaldehyde, gaseous or as aqueous solution, to an aqueous solution of the sulphuric and hydrocyanic acids; the reactants are preferably in approximately stoichiometric proportions. The sulphonic acids may be prepared by passing sulphur trioxide into concentrated aqueous ammonia; by saturating a concentrated hydroxylamine hydrochloride solution with sulphur dioxide; or, as salts, by reacting a concentrated sodium bisulphite solution with sodium nitrite with ice cooling: nitrilosulphonic acid can be obtained from the sodium salt so prepared, and can be hydrolysed to imido sulphonic and amidosulphonic acids. Specification 496,781 is referred to.
GB6367/59A 1958-03-19 1959-02-24 Production of nitrilotriacetonitrile Expired GB851783A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE851783X 1958-03-19

Publications (1)

Publication Number Publication Date
GB851783A true GB851783A (en) 1960-10-19

Family

ID=6782285

Family Applications (1)

Application Number Title Priority Date Filing Date
GB6367/59A Expired GB851783A (en) 1958-03-19 1959-02-24 Production of nitrilotriacetonitrile

Country Status (1)

Country Link
GB (1) GB851783A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3546271A (en) * 1968-06-27 1970-12-08 Hooker Chemical Corp Process for the production of amineacetonitriles

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3546271A (en) * 1968-06-27 1970-12-08 Hooker Chemical Corp Process for the production of amineacetonitriles

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