GB723397A - Production of hydantoin and of glycine - Google Patents

Production of hydantoin and of glycine

Info

Publication number
GB723397A
GB723397A GB29020/52A GB2902052A GB723397A GB 723397 A GB723397 A GB 723397A GB 29020/52 A GB29020/52 A GB 29020/52A GB 2902052 A GB2902052 A GB 2902052A GB 723397 A GB723397 A GB 723397A
Authority
GB
United Kingdom
Prior art keywords
solution
hydantoin
formaldehyde
glycine
alkali metal
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
GB29020/52A
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.)
Dow Chemical Co
Original Assignee
Dow Chemical Co
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 Dow Chemical Co filed Critical Dow Chemical Co
Publication of GB723397A publication Critical patent/GB723397A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D233/00Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/54Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
    • C07D233/66Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D233/72Two oxygen atoms, e.g. hydantoin

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

A process for making hydantoin comprises introducing one molecular proportion of formaldehyde into contact with an aqueous solution containing an ammonium carbonate and an alkali metal cyanide in proportions sufficient to provide the chemical equivalent of at least two mols. of ammonia, and at least 1.5 mols. of carbonate and at least one mol. of the alkali metal p cyanide, maintained at a temperature of from -10 DEG to 30 DEG C., either by slowly adding the formaldehyde in the form of an aqueous solution at a rate such that not more than one mol. of the formaldehyde is released into contact with the dissolved salts in the solution over a period of 4 hours or more or by dissolving a proportionate amount of paraformaldehyde in the solution, then heating the solution at a temperature of from 50 DEG to 120 DEG C. to complete the reaction and form hydantoin. Glycine is prepared by boiling the aqueous reaction liquid to distil ammonia and carbon dioxide, mixing the residual aqueous liquid with an alkali metal hydroxide in amount corresponding to at least two mols. of the alkali metal hydroxide per mol. of the formaldehyde starting material, heating the alkaline solution at a temperature between 130 DEG and 250 DEG C. under pressure to hydrolyse the hydantoin and recovering glycine from the alkaline hydrolysis liquid. Starting materials mentioned include sodium or potassium cyanide and ammonium carbonate or bicarbonate. The alkaline solutions containing hydantoin and glycine are treated with cation exchange resins in hydrogen form to remove alkali metal ions before separating the desired products. Insoluble sulphonated vinyl aromatic resins and sulphonated phenol-formaldehyde resins are mentioned. In examples: hydantoin is obtained by dissolving paraformaldehyde in an aqueous solution containing sodium cyanide and ammonium bicarbonate, boiling the solution, treating it with decolourizing charcoal and a sulphonated vinyl aromatic resin in hydrogen form and concentrating and cooling the residual solution (1); reaction liquor from (1) is heated in an autoclave with sodium hydroxide and the solution is decolourized, boiled, cooled, treated with the ion exchange resin used in (1); concentrated and treated with methyl alcohol to obtain glycine (2); and formaldehyde is gradually added to an aqueous solution of ammonium carbonate and sodium cyanide, the mixture is heated under pressure, ammonia and carbon dioxide are boiled off, aqueous caustic soda is added and the solution is pumped through a heated tube to effect hydrolysis of the hydantoin. The hydrolysed solution is treated with the ion exchange resin used in (1) and concentrated and glycine is precipitated by the addition of methyl alcohol. Specifications 687,486 and 693,522 are referred to. Reference has been directed by the Comptroller to Specifications 687,486 and 693,522.
GB29020/52A 1952-03-22 1952-11-17 Production of hydantoin and of glycine Expired GB723397A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US723397XA 1952-03-22 1952-03-22

Publications (1)

Publication Number Publication Date
GB723397A true GB723397A (en) 1955-02-09

Family

ID=22106969

Family Applications (1)

Application Number Title Priority Date Filing Date
GB29020/52A Expired GB723397A (en) 1952-03-22 1952-11-17 Production of hydantoin and of glycine

Country Status (1)

Country Link
GB (1) GB723397A (en)

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