GB910334A - Process for producing organosilicon compounds - Google Patents

Process for producing organosilicon compounds

Info

Publication number
GB910334A
GB910334A GB4192160A GB4192160A GB910334A GB 910334 A GB910334 A GB 910334A GB 4192160 A GB4192160 A GB 4192160A GB 4192160 A GB4192160 A GB 4192160A GB 910334 A GB910334 A GB 910334A
Authority
GB
United Kingdom
Prior art keywords
catalyst
starting material
yield
water
radicals
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
GB4192160A
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.)
Union Carbide Corp
Original Assignee
Union Carbide Corp
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 Union Carbide Corp filed Critical Union Carbide Corp
Publication of GB910334A publication Critical patent/GB910334A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G77/00Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
    • C08G77/04Polysiloxanes
    • C08G77/06Preparatory processes
    • C08G77/08Preparatory processes characterised by the catalysts used
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G77/00Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Silicon Polymers (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)

Abstract

Organosilicon compounds of the formula <FORM:0910334/IV(a)/1> wherein each R is a mono-valent hydrocarbon radical (saturated or unsaturated) with or without, as substituent, a halogen atom, or an amino, hydroxyl, cyano, carbalkoxy, aminoalkylamino, alkoxy or aryloxy group, R1 is an alkyl radical or H atom and n is at least 1, are condensed in the presence of a catalytic amount of a compound of the formula (R11COO)aM, wherein M is Hg, Th or Pb, a has the value of the valency of M and R11 is a monovalent aliphatic hydrocarbon radical. Preferably the salts are derived from alkanoic acids of 2 to 10 C atoms, e.g. mercuric, acetates, lead and thallous propanoates, butanoates and octoates. The catalyst is generally used in amount from 0,01 to 20% by weight of the starting material and the process can be effected at a temperature from 25 DEG to 170 DEG C. with continuous removal of water or water and alcohol produced as a by-product. If desired the starting material and catalyst may be dissolved in an inert solvent. After completion of the reaction the catalyst may be removed, such as by washing with water. The products may be oils or gums, and intermediate products containing Si-bonded OH or OR groups may be end-blocked by reacting with trihydrocarbon-halo-silanes. If desired, alkoxysilanes may be co-condensed with the starting material to yield siloxanes containing functional groups. Products containing alkenyl radicals can be cured through these radicals to yield gums, and products containing alkoxy radicals can be hydrolysed to yield resins. In a typical example (1) a mixture of HO[(CH3)2SiO]H20 and mercuric acetate was heated at 150 DEG C. for 40 hours to give a siloxane gum. Uses: For producing elastomers, and as hydraulic fluids.
GB4192160A 1959-12-08 1960-12-06 Process for producing organosilicon compounds Expired GB910334A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US85804859A 1959-12-08 1959-12-08

Publications (1)

Publication Number Publication Date
GB910334A true GB910334A (en) 1962-11-14

Family

ID=25327349

Family Applications (1)

Application Number Title Priority Date Filing Date
GB4192160A Expired GB910334A (en) 1959-12-08 1960-12-06 Process for producing organosilicon compounds

Country Status (2)

Country Link
DE (1) DE1243395B (en)
GB (1) GB910334A (en)

Also Published As

Publication number Publication date
DE1243395B (en) 1967-06-29

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