GB946835A - New organic silicates - Google Patents

New organic silicates

Info

Publication number
GB946835A
GB946835A GB9673/61A GB967361A GB946835A GB 946835 A GB946835 A GB 946835A GB 9673/61 A GB9673/61 A GB 9673/61A GB 967361 A GB967361 A GB 967361A GB 946835 A GB946835 A GB 946835A
Authority
GB
United Kingdom
Prior art keywords
alkyl
aryl
aryl group
orthosilicate
tetra
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
GB9673/61A
Inventor
Brian Beard Millward
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.)
Monsanto Chemicals Ltd
Original Assignee
Monsanto Chemicals Ltd
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 Monsanto Chemicals Ltd filed Critical Monsanto Chemicals Ltd
Priority to GB9673/61A priority Critical patent/GB946835A/en
Priority to FR890939A priority patent/FR1317620A/fr
Priority to FR891101A priority patent/FR81295E/en
Publication of GB946835A publication Critical patent/GB946835A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F7/00Compounds containing elements of Groups 4 or 14 of the Periodic Table
    • C07F7/02Silicon compounds
    • C07F7/04Esters of silicic acids
    • C07F7/06Esters of silicic acids with hydroxyaryl compounds
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2/00Processes or devices for granulating materials, e.g. fertilisers in general; Rendering particulate materials free flowing in general, e.g. making them hydrophobic
    • B01J2/28Processes or devices for granulating materials, e.g. fertilisers in general; Rendering particulate materials free flowing in general, e.g. making them hydrophobic using special binding agents
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F7/00Compounds containing elements of Groups 4 or 14 of the Periodic Table
    • C07F7/02Silicon compounds
    • C07F7/08Compounds having one or more C—Si linkages
    • C07F7/18Compounds having one or more C—Si linkages as well as one or more C—O—Si linkages
    • C07F7/1804Compounds having Si-O-C linkages
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F7/00Compounds containing elements of Groups 4 or 14 of the Periodic Table
    • C07F7/02Silicon compounds
    • C07F7/08Compounds having one or more C—Si linkages
    • C07F7/18Compounds having one or more C—Si linkages as well as one or more C—O—Si linkages
    • C07F7/1804Compounds having Si-O-C linkages
    • C07F7/1872Preparation; Treatments not provided for in C07F7/20
    • C07F7/188Preparation; Treatments not provided for in C07F7/20 by reactions involving the formation of Si-O linkages
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M3/00Liquid compositions essentially based on lubricating components other than mineral lubricating oils or fatty oils and their use as lubricants; Use as lubricants of single liquid substances
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2227/00Organic non-macromolecular compounds containing atoms of elements not provided for in groups C10M2203/00, C10M2207/00, C10M2211/00, C10M2215/00, C10M2219/00 or C10M2223/00 as ingredients in lubricant compositions
    • C10M2227/02Esters of silicic acids
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/08Hydraulic fluids, e.g. brake-fluids

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)

Abstract

Aryl silicates are prepared by reacting a silicon halide with an alkali metal salt of a phenol that is substituted by an alkyl group in each of the two positions ortho to the hydroxyl group. The products include new compounds of the formula (XO)nSi Y4-n where X is an aryl group substituted in the two ortho positions by alkyl, Y is an aryl group, and n is 1 to 4; when n is 4 the two o-alkyl groups are methyl. Specified silicon halides are SiCl4, SiB4, SiI4 and PhSiCl3, and others such as diaryl-dihalo-, triarylhalo- and trihalo-silanes may be used. Specified phenols are 2,6-dimethyl-, 2,4,6-trimethyl-, 2,6-diethyl, and 2-ethyl-6-methyl-phenols and 1,3-dimethyl-beta-naphthol. The salt is preferably sodium. The aryl group can carry additional inert substituents e.g. alkyl, aryl and aryloxy groups Anhydrous conditions are necessary in the preparation. Examples describe the preparation of (1) tetra (2,6-dimethylphenyl) orthosilicate; (2) tetra (2,4,6-trimethylphenyl) orthosilicate; (3) phenyltri (2,6,-dimethylphenoxy) silane.
GB9673/61A 1961-03-16 1961-03-16 New organic silicates Expired GB946835A (en)

Priority Applications (3)

Application Number Priority Date Filing Date Title
GB9673/61A GB946835A (en) 1961-03-16 1961-03-16 New organic silicates
FR890939A FR1317620A (en) 1961-03-16 1962-03-13
FR891101A FR81295E (en) 1961-03-16 1962-03-14 New organic silicates

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB9673/61A GB946835A (en) 1961-03-16 1961-03-16 New organic silicates

Publications (1)

Publication Number Publication Date
GB946835A true GB946835A (en) 1964-01-15

Family

ID=9876549

Family Applications (1)

Application Number Title Priority Date Filing Date
GB9673/61A Expired GB946835A (en) 1961-03-16 1961-03-16 New organic silicates

Country Status (2)

Country Link
FR (1) FR1317620A (en)
GB (1) GB946835A (en)

Also Published As

Publication number Publication date
FR1317620A (en) 1963-05-08

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