GB650493A - Manufacture of alkyl xanthogenate glycol formates - Google Patents

Manufacture of alkyl xanthogenate glycol formates

Info

Publication number
GB650493A
GB650493A GB13313/48A GB1331348A GB650493A GB 650493 A GB650493 A GB 650493A GB 13313/48 A GB13313/48 A GB 13313/48A GB 1331348 A GB1331348 A GB 1331348A GB 650493 A GB650493 A GB 650493A
Authority
GB
United Kingdom
Prior art keywords
xanthate
chloroformate
glycol
bis
sodium
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
GB13313/48A
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.)
Wyeth Holdings LLC
Original Assignee
American Cyanamid 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 American Cyanamid Co filed Critical American Cyanamid Co
Publication of GB650493A publication Critical patent/GB650493A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C329/00Thiocarbonic acids; Halides, esters or anhydrides thereof
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B03SEPARATION OF SOLID MATERIALS USING LIQUIDS OR USING PNEUMATIC TABLES OR JIGS; MAGNETIC OR ELECTROSTATIC SEPARATION OF SOLID MATERIALS FROM SOLID MATERIALS OR FLUIDS; SEPARATION BY HIGH-VOLTAGE ELECTRIC FIELDS
    • B03DFLOTATION; DIFFERENTIAL SEDIMENTATION
    • B03D1/00Flotation
    • B03D1/001Flotation agents
    • B03D1/004Organic compounds
    • B03D1/012Organic compounds containing sulfur
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B03SEPARATION OF SOLID MATERIALS USING LIQUIDS OR USING PNEUMATIC TABLES OR JIGS; MAGNETIC OR ELECTROSTATIC SEPARATION OF SOLID MATERIALS FROM SOLID MATERIALS OR FLUIDS; SEPARATION BY HIGH-VOLTAGE ELECTRIC FIELDS
    • B03DFLOTATION; DIFFERENTIAL SEDIMENTATION
    • B03D2201/00Specified effects produced by the flotation agents
    • B03D2201/02Collectors
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B03SEPARATION OF SOLID MATERIALS USING LIQUIDS OR USING PNEUMATIC TABLES OR JIGS; MAGNETIC OR ELECTROSTATIC SEPARATION OF SOLID MATERIALS FROM SOLID MATERIALS OR FLUIDS; SEPARATION BY HIGH-VOLTAGE ELECTRIC FIELDS
    • B03DFLOTATION; DIFFERENTIAL SEDIMENTATION
    • B03D2203/00Specified materials treated by the flotation agents; specified applications
    • B03D2203/02Ores
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B03SEPARATION OF SOLID MATERIALS USING LIQUIDS OR USING PNEUMATIC TABLES OR JIGS; MAGNETIC OR ELECTROSTATIC SEPARATION OF SOLID MATERIALS FROM SOLID MATERIALS OR FLUIDS; SEPARATION BY HIGH-VOLTAGE ELECTRIC FIELDS
    • B03DFLOTATION; DIFFERENTIAL SEDIMENTATION
    • B03D2203/00Specified materials treated by the flotation agents; specified applications
    • B03D2203/02Ores
    • B03D2203/025Precious metal ores

Landscapes

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

Abstract

Xanthate derivatives, termed alkyl xanthogenate glycol formates, are prepared by reacting one mol. of a glycol chloroformate containing two chloroformate radicals with at least one and not more than two mols. of an alkali metal alkyl xanthate. According to one method, an alkali metal alkyl xanthate is slurried in an inert organic liquid such as ether or benzene and the glycol chloroformate is added slowly at a low temperature, e.g. below 5 DEG C.; inorganic salts are then filtered off or leached out with water and the solvent distilled off. Alternatively, the xanthate is added directly to the chloroformate, preferably at below 40 DEG C., followed by washing or drying. In a third process, the chloroformate is added to a cold water solution of the xanthate at about 5 DEG C. and the product which separates out as an oil is removed and dried. Mixtures of xanthates may be used. The products, derived from diglycol chloroformate for illustrative purposes may have the general formula <FORM:0650493/IV (b)/1> or <FORM:0650493/IV (b)/2> where R=alkyl, depending on whether one or two mols. of xanthate are employed. The compounds may be used as flotation reagents, in which connection reference is made to Specification 650,498, [Group II]. In examples, the following compounds are interacted, using one or other of the above methods and in molecular proportions of xanthate to chloroformate of 1 : 1 or 2 : 1, (1) sodium ethyl xanthate, sodium sec.-butyl xanthate, sodium isopropyl xanthate and potassium amyl xanthate, respectively, with diglycol bis.-chloroformate; (2) sodium isopropyl xanthate, sodium ethyl xanthate and potassium amyl xanthate, respectively, with ethylene glycol bis-chloroformate; (3) sodium isopropyl xanthate with trimethylene glycol bis-chloroformate or dipropylene glycol bischloroformate; (4) sodium ethyl xanthate with octadecane diol bis-chloroformate (prepared by action of phosgene in carbon tetrachloride on the diol), triethylene glycol bis-chloroformate and butine-2-diol-1 : 4 bis-chloroformate, respectively. The Specification as open to inspection under Sect. 91 states that the glycol chloroformates may be reacted with at least one mol. of alkali metal xanthate. This subject-matter does not appear in the Specification as accepted.
GB13313/48A 1947-06-25 1948-05-14 Manufacture of alkyl xanthogenate glycol formates Expired GB650493A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US650493XA 1947-06-25 1947-06-25

Publications (1)

Publication Number Publication Date
GB650493A true GB650493A (en) 1951-02-28

Family

ID=22060011

Family Applications (1)

Application Number Title Priority Date Filing Date
GB13313/48A Expired GB650493A (en) 1947-06-25 1948-05-14 Manufacture of alkyl xanthogenate glycol formates

Country Status (1)

Country Link
GB (1) GB650493A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE931468C (en) * 1952-08-14 1955-08-08 Huels Chemische Werke Ag Process for the production of sulfur-containing condensation products

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE931468C (en) * 1952-08-14 1955-08-08 Huels Chemische Werke Ag Process for the production of sulfur-containing condensation products

Similar Documents

Publication Publication Date Title
ES2122296T3 (en) FLUORATED BIS-ETERS AND PROCEDURE FOR THE PREPARATION OF SUCH FLUORATED METHYL ETERS AND ETHERS.
GB476727A (en) Improvements in the manufacture and production of interpolymerisation products
US2047066A (en) Softening agent
GB650493A (en) Manufacture of alkyl xanthogenate glycol formates
US2138917A (en) Production of high molecular glycols and esters thereof
US2345061A (en) Organic compound and process for producing the same
GB604388A (en) Improvements in or relating to extreme pressure lubricating oil compositions
US3365402A (en) Process for eliminating the harmful effects of an alkaline catalyst in capillary-active products
US2418942A (en) Method for producing polymeric materials containing sulfur
US2036423A (en) Sulphonic acid esters of cellulose derivatives and the preparation thereof
GB467579A (en) Improvements in the removal of gaseous weak acids from gases containing the same
US2337532A (en) Alkyl derivatives of benzenesulphonyl fluoride
US2185654A (en) Process for the production of sulphonium sulphonates
US2378551A (en) Process for producing condensation products
US2497135A (en) Polymeric sulfurous acid esters
US2608572A (en) Xanthogen formates
GB855714A (en) Halogenated and/or sulphohalogenated copolymers of lower olefines and process for their manufacture
GB159153A (en) Process for the preparation of di-substituted 2-4-diketo-tetra-hydro-oxazoles
US2050169A (en) High-molecular sulphur compounds and process of manufacturing the same
US1852110A (en) Method of making xanthates
GB662477A (en) Process for making alkyl esters of aryl sulfonic acid
GB950254A (en) Process for the manufacture of n-phenyl-n-alkoxy-n-alkyl ureas and substitution products thereof
GB493513A (en) Production of new derivatives of starch
US2835694A (en) Alkyl n-methyl-n-(2-sulfoethyl) carbamoyl derivatives of carbocyclic 1, 2-carboxylicacids
US2163238A (en) Process for the manufacture of polymer carboxylic acids and derivatives thereof