WO1997008176A1 - Compose de silane et son procede de preparation - Google Patents

Compose de silane et son procede de preparation Download PDF

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Publication number
WO1997008176A1
WO1997008176A1 PCT/JP1996/002363 JP9602363W WO9708176A1 WO 1997008176 A1 WO1997008176 A1 WO 1997008176A1 JP 9602363 W JP9602363 W JP 9602363W WO 9708176 A1 WO9708176 A1 WO 9708176A1
Authority
WO
WIPO (PCT)
Prior art keywords
reaction
silane compound
sec
compound
mol
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.)
Ceased
Application number
PCT/JP1996/002363
Other languages
English (en)
French (fr)
Japanese (ja)
Inventor
Takayuki Taki
Masashi Nakajima
Kunihiko Imanishi
Masahide Murata
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.)
Tonen General Sekiyu KK
Original Assignee
Tonen 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 Tonen Corp filed Critical Tonen Corp
Priority to US09/029,268 priority Critical patent/US5856549A/en
Priority to EP96927889A priority patent/EP0852228A1/en
Publication of WO1997008176A1 publication Critical patent/WO1997008176A1/ja
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

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Classifications

    • 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 Table
    • 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

Definitions

  • the present invention relates to a novel silane compound and a method for producing the same, and more particularly, to a silane polymerization catalyst component, a silane coupling agent, and the like.
  • the present invention relates to a novel silane compound used and a method for producing the same.
  • the present invention provides a novel catalyst useful as a propylene polymerization catalyst component having a high activity and a high stereoregularity, or a silane coupling agent.
  • the purpose is to provide lan compounds and their production methods.
  • the present invention is a.
  • the present invention provides a method for producing a novel silane compound represented by the above formula (I). That is, n-produced trihalosilane is reacted with sec-butanol, and then the resulting reactant is reacted with methanol. Thus, the silane compound of the above formula (I) is produced.
  • FIG. 1 is an iH-NMR chart of di-sec-butoxy-n-propylmethoxysilane produced in Example 1. The curves above the peaks and the numbers below the peaks indicate the area intensity of each peak.
  • FIG. 2 is an IR chart of the di-sec-butoxy-n-propylmethoxysilane produced in Example 1. BEST MODE FOR CARRYING OUT THE INVENTION
  • This silane compound (I) has a boiling point of 125 ° C / 0.1 mmHg. The structure of this silane compound can be confirmed by GC-MS, 1 ⁇ 2-NMR, infrared absorption spectrum (IR), and the like.
  • this silane compound (I) is used as a catalyst component, a olefin-based polymer such as polypropylene or polybutene having a high stereoregularity can be obtained. Can be produced under high polymerization activity.
  • this silane compound (I) Since this silane compound (I) has a hydrolyzable group, it is used as a silane coupling agent, a polymerizable monomer and a resin modifier. Can be used.
  • n-propyltrihalosilane as a raw material is represented by the following formula (II):
  • trihalosilane H—Six 3
  • 0.9 to 1.1 moles of trihalosilane per mole of propylene use 0.9 to 1.1 moles of trihalosilane per mole of propylene.
  • the reaction conditions are, for example, at a temperature of 100 to 200, for 10 minutes to 10 hours, and a platinum-based catalyst such as chloroplatinic acid, platinum-1,1,3,3-te. It is preferable to use a tramethyl-1,3-divinyldisiloxane complex or the like.
  • a solvent can be used, and examples thereof include benzene and toluene.
  • n-Propyl peroxylan is also commercially available, and in the present invention, those commercially available products can also be used.
  • reaction B When performing the above reaction B, use 2 to 2.5 moles of sec-butanol based on 1 n-propyltrihalosilane (II).
  • the reaction is for example, it is carried out at a temperature of 0 to 100 ° C. for 10 minutes to 5 hours, preferably at a temperature of 10 to 70 ° C. for 30 minutes to 4 hours.
  • Solvents can also be used, for example, organic solvents such as hexane, ether, petroleum ether, benzene, etc.
  • halogenated hydrogen acceptor examples include tertiary amines such as triethylamine and nitrogen-containing heterocyclic compounds such as pyridin, quinoline and isoquinoline. Lin etc. are mentioned. Of these, pyridine and quinoline are preferably used.
  • the halogenated hydrogen acceptor is preferably used in an amount of 2 to 2.5 mol per 1 mol of n-provindolinodoxylan.
  • the above-mentioned silane compound (I) of the present invention is produced by reacting compound (III) with methanol.
  • the methanol is added in an amount of 1 to 2 with respect to 1 mol of the compound (III). Use moles.
  • the reaction is carried out at a temperature of 0 to 100 ° C for 10 minutes to 5 hours, preferably at a temperature of 10 to 70 ° C for 30 minutes to 2 hours.
  • a hydrogen hydride acceptor in order to promptly progress the reaction.
  • the hydrogen halide acceptor the hydrogen halide acceptor exemplified in Reaction B above can be used.
  • the hydrogen halide acceptor used here may be the same as or different from the compound used in the previous reaction, but usually the same is used.
  • the hydrogen halide acceptor is preferably used in an amount of 1 to 2 mol per 1 mol of the compound (III).
  • reaction B and reaction C by blowing an inert gas, the generated hydrogen halide is removed from the reaction system, and the reaction is allowed to proceed rapidly. You can do it.
  • a novel silane compound (I) can be obtained in high yield by the above-mentioned production method.
  • the salt formed was removed by filtration, then the hexane was distilled off, and then the mixture was distilled under reduced pressure to obtain a liquid having a boiling point of 125 ° C Z0.
  • Measurement apparatus HITACHIR 1 5 0 0 ((Ltd.) Hitachi) Measurement solvent: CD 3 C 1, standard residual click B port E Lum
  • Measuring device 160 Series F T-IR (PerkinElmer) Measuring method: Liquid film method (KBr plate)
  • a novel silane compound useful as a propylene polymerization catalyst component, a silane coupling agent, and the like, and a method for producing the same are provided.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
PCT/JP1996/002363 1995-08-24 1996-08-23 Compose de silane et son procede de preparation Ceased WO1997008176A1 (fr)

Priority Applications (2)

Application Number Priority Date Filing Date Title
US09/029,268 US5856549A (en) 1995-08-24 1996-08-23 Silane compound and process for the preparation thereof
EP96927889A EP0852228A1 (en) 1995-08-24 1996-08-23 Silane compound and process for the preparation thereof

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP23924795A JP3398266B2 (ja) 1995-08-24 1995-08-24 シラン化合物及びその製造方法
JP7/239247 1995-08-24

Publications (1)

Publication Number Publication Date
WO1997008176A1 true WO1997008176A1 (fr) 1997-03-06

Family

ID=17041929

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/JP1996/002363 Ceased WO1997008176A1 (fr) 1995-08-24 1996-08-23 Compose de silane et son procede de preparation

Country Status (4)

Country Link
US (1) US5856549A (OSRAM)
EP (1) EP0852228A1 (OSRAM)
JP (1) JP3398266B2 (OSRAM)
WO (1) WO1997008176A1 (OSRAM)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2841244B1 (fr) * 2002-06-21 2007-10-05 Rhodia Chimie Sa Procede de preparation d'organo dialkylalcoxysilane
DE102004025766A1 (de) * 2004-05-26 2005-12-22 Degussa Ag Herstellung von Organosilanestern
JP4803395B2 (ja) * 2007-06-19 2011-10-26 信越化学工業株式会社 ヒドロキシル基のシリル化方法

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5920291A (ja) * 1982-07-01 1984-02-01 アライド・コ−ポレ−シヨン アルコキシシランの製造法
JPH0532718A (ja) * 1991-01-26 1993-02-09 Basf Ag ツイーグラー触媒系のためのバナジウムおよびマグネシウム含有組成分
JPH0820646A (ja) * 1994-07-06 1996-01-23 Shin Etsu Chem Co Ltd 加水分解性官能基含有オルガノポリシロキサンの製造方法及び硬化性樹脂組成物
JPH08134128A (ja) * 1994-11-15 1996-05-28 Tonen Corp ポリオレフィン製造用触媒
JPH08134129A (ja) * 1994-11-15 1996-05-28 Tonen Corp ポリオレフィン製造用触媒

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5248803A (en) * 1991-10-16 1993-09-28 Tonen Corporation Silane compound and processes for the preparation thereof
JP2938726B2 (ja) * 1993-09-10 1999-08-25 信越化学工業株式会社 第３級ブチルシクロアルキルジアルコキシシラン化合物の製造方法
DE69600346T2 (de) * 1995-03-28 1998-12-17 Tonen Corp., Tokio/Tokyo Katalysator für die Olefinpolymerisation und Verfahren zur Olefinpolymerisation unter Anwendung desselben

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5920291A (ja) * 1982-07-01 1984-02-01 アライド・コ−ポレ−シヨン アルコキシシランの製造法
JPH0532718A (ja) * 1991-01-26 1993-02-09 Basf Ag ツイーグラー触媒系のためのバナジウムおよびマグネシウム含有組成分
JPH0820646A (ja) * 1994-07-06 1996-01-23 Shin Etsu Chem Co Ltd 加水分解性官能基含有オルガノポリシロキサンの製造方法及び硬化性樹脂組成物
JPH08134128A (ja) * 1994-11-15 1996-05-28 Tonen Corp ポリオレフィン製造用触媒
JPH08134129A (ja) * 1994-11-15 1996-05-28 Tonen Corp ポリオレフィン製造用触媒

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See also references of EP0852228A4 *

Also Published As

Publication number Publication date
US5856549A (en) 1999-01-05
EP0852228A4 (OSRAM) 1998-07-29
JPH0959284A (ja) 1997-03-04
JP3398266B2 (ja) 2003-04-21
EP0852228A1 (en) 1998-07-08

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