GB1292077A - Organosilicon compounds - Google Patents

Organosilicon compounds

Info

Publication number
GB1292077A
GB1292077A GB3611870A GB3611870A GB1292077A GB 1292077 A GB1292077 A GB 1292077A GB 3611870 A GB3611870 A GB 3611870A GB 3611870 A GB3611870 A GB 3611870A GB 1292077 A GB1292077 A GB 1292077A
Authority
GB
United Kingdom
Prior art keywords
formula
methyloxypropyl
methacryloxypropyl
trichlorosilane
trimethoxysilane
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
GB3611870A
Inventor
Hans-Joachim Vahlensieck
Claus-Dieter Seiler
Hans-Joachim Kotzsch
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.)
Dynamit Nobel AG
Original Assignee
Dynamit Nobel AG
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 Dynamit Nobel AG filed Critical Dynamit Nobel AG
Publication of GB1292077A publication Critical patent/GB1292077A/en
Expired legal-status Critical Current

Links

Classifications

    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/16—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
    • B01J31/22—Organic complexes
    • B01J31/2204—Organic complexes the ligands containing oxygen or sulfur as complexing atoms
    • B01J31/2208—Oxygen, e.g. acetylacetonates
    • B01J31/2226—Anionic ligands, i.e. the overall ligand carries at least one formal negative charge
    • B01J31/223—At least two oxygen atoms present in one at least bidentate or bridging ligand
    • B01J31/2234—Beta-dicarbonyl ligands, e.g. acetylacetonates
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic System
    • C07F7/02—Silicon compounds
    • C07F7/08—Compounds having one or more C—Si linkages
    • C07F7/12—Organo silicon halides
    • C07F7/14—Preparation thereof from optionally substituted halogenated silanes and hydrocarbons hydrosilylation reactions
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic System
    • C07F7/02—Silicon compounds
    • C07F7/08—Compounds having one or more C—Si linkages
    • C07F7/18—Compounds having one or more C—Si linkages as well as one or more C—O—Si linkages
    • C07F7/1804—Compounds having Si-O-C linkages
    • C07F7/1872—Preparation; Treatments not provided for in C07F7/20
    • C07F7/1876—Preparation; Treatments not provided for in C07F7/20 by reactions involving the formation of Si-C linkages
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2231/00—Catalytic reactions performed with catalysts classified in B01J31/00
    • B01J2231/30—Addition reactions at carbon centres, i.e. to either C-C or C-X multiple bonds
    • B01J2231/32—Addition reactions to C=C or C-C triple bonds
    • B01J2231/323—Hydrometalation, e.g. bor-, alumin-, silyl-, zirconation or analoguous reactions like carbometalation, hydrocarbation
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2531/00—Additional information regarding catalytic systems classified in B01J31/00
    • B01J2531/80—Complexes comprising metals of Group VIII as the central metal
    • B01J2531/82—Metals of the platinum group
    • B01J2531/828—Platinum
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/16—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
    • B01J31/22—Organic complexes
    • B01J31/2282—Unsaturated compounds used as ligands
    • B01J31/2291—Olefins

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Inorganic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)

Abstract

1292077 Silanes DYNAMIT NOBEL AG 24 July 1970 [25 July 1969] 36118/70 Heading C3S Novel silanes of the formula (wherein R<SP>11</SP> represents an alkyl group) and other organosilicon compounds are prepared by reacting a silane of the formula H a SiR b X 4- ( a+b ), in which X represents halogen, alkoxy, or aryloxy, R reprssents halogen, alkoxy, aryloxy, alkyl, cycloalkyl or aryl, a is 1 or 2 and b is 0 or 1, with an ethylenically or acetylenically unsaturated compound in the presence of a platinum catalyst of the formula [PtR<SP>1</SP>Cl 2 ] c in which R<SP>1</SP> represents a molecule of an unsaturated ketone and c is 1 or 2. Examples describe the preparation of gamma-glycidyloxypropyltrimethoxysilane, 3 - acetyl - oxypropyl - trichlorosilane, 3 - (2<SP>1</SP> - ethylcaproyloxy) - propyltriethoxysilane, 3 - methacryloxypropyl - trichlorosilane, 3 - methacryloxypropyl - trimethoxysilane, 3 - tetrahydrofurfuryl - 2 - methyloxypropyl - triethoxysilane, 3 - tetrahydrofurfuryl - 2 - methyloxypropyl - trimethoxysilane and the conversionof the latter to the corresponding triethoxysilane derivative by reaction with ethanol. Uses.-As resin additives, in glass dressings and finishes, for treating metals, minerals, wood, textiles and paper, and as bonding agents between polymers and glass.
GB3611870A 1969-07-25 1970-07-24 Organosilicon compounds Expired GB1292077A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE19691937904 DE1937904C3 (en) 1969-07-25 1969-07-25 Process for the preparation of organosilicon compounds by addition

Publications (1)

Publication Number Publication Date
GB1292077A true GB1292077A (en) 1972-10-11

Family

ID=5740912

Family Applications (1)

Application Number Title Priority Date Filing Date
GB3611870A Expired GB1292077A (en) 1969-07-25 1970-07-24 Organosilicon compounds

Country Status (11)

Country Link
JP (1) JPS4925651B1 (en)
AT (1) AT300839B (en)
BE (1) BE753898A (en)
CH (1) CH542884A (en)
DE (1) DE1937904C3 (en)
FI (1) FI51592C (en)
FR (1) FR2055613A5 (en)
GB (1) GB1292077A (en)
NL (1) NL7010996A (en)
NO (1) NO133404C (en)
SE (1) SE369723B (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2159991C2 (en) * 1971-12-03 1982-10-21 Dynamit Nobel Ag, 5210 Troisdorf Silicon-containing dioxolane derivatives
JPH01501144A (en) * 1986-10-21 1989-04-20 インスティテュト　オルガニチェスコゴ　シンテザ　アカデミイ　ナウク　ラトビースコイ　エスエスアール 2,6-dimethyl-3,5-dimethoxycarbonyl-4-(5'-trimethylsilyl-2'-furyl)-1,4-dihydropyridine

Also Published As

Publication number Publication date
BE753898A (en) 1970-12-31
NO133404C (en) 1976-04-28
NL7010996A (en) 1971-01-27
FI51592B (en) 1976-11-01
DE1937904B2 (en) 1974-10-10
DE1937904A1 (en) 1971-02-25
FR2055613A5 (en) 1971-05-07
FI51592C (en) 1977-02-10
JPS4925651B1 (en) 1974-07-02
AT300839B (en) 1972-08-10
DE1937904C3 (en) 1975-05-28
CH542884A (en) 1973-11-30
SE369723B (en) 1974-09-16
NO133404B (en) 1976-01-19

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Legal Events

Date Code Title Description
PS Patent sealed
PE20 Patent expired after termination of 20 years