JPS6138197B2 - - Google Patents

Info

Publication number: JPS6138197B2
Authority: JP; Japan
Prior art keywords: group; reaction; organic; present; general formula
Prior art date: 1978-10-05
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

JP53122801A

Other languages

English (en)

Japanese (ja)

Other versions

JPS5549387A (en

Inventor

Tetsuyoshi Suzuki

Sunao Imaki

Takezo Nakanome

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.)

Mitsubishi Chemical Corp

Original Assignee

Mitsubishi Chemical Industries 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.)

1978-10-05

Filing date

1978-10-05

Publication date

1986-08-28

1978-10-05 Application filed by Mitsubishi Chemical Industries Ltd filed Critical Mitsubishi Chemical Industries Ltd

1978-10-05 Priority to JP12280178A priority Critical patent/JPS5549387A/ja

1980-04-09 Publication of JPS5549387A publication Critical patent/JPS5549387A/ja

1986-08-28 Publication of JPS6138197B2 publication Critical patent/JPS6138197B2/ja

Status Granted legal-status Critical Current

Links

125000000217 alkyl group Chemical group 0.000 claims description 7
125000004432 carbon atom Chemical group C* 0.000 claims description 7
125000005678 ethenylene group Chemical group [H]C([*:1])=C([H])[*:2] 0.000 claims description 4
125000000816 ethylene group Chemical group [H]C([H])([*:1])C([H])([H])[*:2] 0.000 claims description 4
125000004183 alkoxy alkyl group Chemical group 0.000 claims description 3
-1 organosilane compounds Chemical class 0.000 description 23
238000006243 chemical reaction Methods 0.000 description 13
239000003054 catalyst Substances 0.000 description 12
229910000077 silane Inorganic materials 0.000 description 11
BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 9
KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 8
239000006087 Silane Coupling Agent Substances 0.000 description 8
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 6
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
239000011368 organic material Substances 0.000 description 6
239000002904 solvent Substances 0.000 description 6
239000011147 inorganic material Substances 0.000 description 5
KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 4
IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 4
238000000921 elemental analysis Methods 0.000 description 4
238000002329 infrared spectrum Methods 0.000 description 4
239000011256 inorganic filler Substances 0.000 description 4
229910003475 inorganic filler Inorganic materials 0.000 description 4
229910052751 metal Inorganic materials 0.000 description 4
239000002184 metal Substances 0.000 description 4
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 4
238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 4
229910052763 palladium Inorganic materials 0.000 description 4
229910052697 platinum Inorganic materials 0.000 description 4
239000000126 substance Substances 0.000 description 4
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
239000010425 asbestos Substances 0.000 description 3
150000001732 carboxylic acid derivatives Chemical class 0.000 description 3
239000002131 composite material Substances 0.000 description 3
229910052895 riebeckite Inorganic materials 0.000 description 3
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
239000002253 acid Substances 0.000 description 2
150000001338 aliphatic hydrocarbons Chemical class 0.000 description 2
PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 2
150000004945 aromatic hydrocarbons Chemical class 0.000 description 2
239000007795 chemical reaction product Substances 0.000 description 2
150000001875 compounds Chemical class 0.000 description 2
239000003365 glass fiber Substances 0.000 description 2
229910052739 hydrogen Inorganic materials 0.000 description 2
239000001257 hydrogen Substances 0.000 description 2
229910010272 inorganic material Inorganic materials 0.000 description 2
238000004519 manufacturing process Methods 0.000 description 2
238000000034 method Methods 0.000 description 2
239000000203 mixture Substances 0.000 description 2
YJVFFLUZDVXJQI-UHFFFAOYSA-L palladium(ii) acetate Chemical compound [Pd+2].CC([O-])=O.CC([O-])=O YJVFFLUZDVXJQI-UHFFFAOYSA-L 0.000 description 2
125000001424 substituent group Chemical group 0.000 description 2
YUYCVXFAYWRXLS-UHFFFAOYSA-N trimethoxysilane Chemical compound CO[SiH](OC)OC YUYCVXFAYWRXLS-UHFFFAOYSA-N 0.000 description 2
125000004200 2-methoxyethyl group Chemical group [H]C([H])([H])OC([H])([H])C([H])([H])* 0.000 description 1
VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
239000005909 Kieselgur Substances 0.000 description 1
229910019142 PO4 Inorganic materials 0.000 description 1
239000004698 Polyethylene Substances 0.000 description 1
239000004743 Polypropylene Substances 0.000 description 1
KJTLSVCANCCWHF-UHFFFAOYSA-N Ruthenium Chemical compound [Ru] KJTLSVCANCCWHF-UHFFFAOYSA-N 0.000 description 1
BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 1
238000009835 boiling Methods 0.000 description 1
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
239000000969 carrier Substances 0.000 description 1
229910052804 chromium Inorganic materials 0.000 description 1
239000011651 chromium Substances 0.000 description 1
229910017052 cobalt Inorganic materials 0.000 description 1
239000010941 cobalt Substances 0.000 description 1
GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
229910052802 copper Inorganic materials 0.000 description 1
239000010949 copper Substances 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
239000011521 glass Substances 0.000 description 1
238000005984 hydrogenation reaction Methods 0.000 description 1
125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
238000000465 moulding Methods 0.000 description 1
229910052759 nickel Inorganic materials 0.000 description 1
RDOHPVPONNHSPH-UHFFFAOYSA-N octa-2,7-dienyl acetate Chemical compound CC(=O)OCC=CCCCC=C RDOHPVPONNHSPH-UHFFFAOYSA-N 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
229910052762 osmium Inorganic materials 0.000 description 1
SYQBFIAQOQZEGI-UHFFFAOYSA-N osmium atom Chemical compound [Os] SYQBFIAQOQZEGI-UHFFFAOYSA-N 0.000 description 1
JKDRQYIYVJVOPF-FDGPNNRMSA-L palladium(ii) acetylacetonate Chemical compound [Pd+2].C\C([O-])=C\C(C)=O.C\C([O-])=C\C(C)=O JKDRQYIYVJVOPF-FDGPNNRMSA-L 0.000 description 1
235000021317 phosphate Nutrition 0.000 description 1
150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
CLSUSRZJUQMOHH-UHFFFAOYSA-L platinum dichloride Chemical compound Cl[Pt]Cl CLSUSRZJUQMOHH-UHFFFAOYSA-L 0.000 description 1
229920000573 polyethylene Polymers 0.000 description 1
229920005672 polyolefin resin Polymers 0.000 description 1
229920001155 polypropylene Polymers 0.000 description 1
QPINXQCQOKBINJ-UHFFFAOYSA-K potassium;platinum(2+);trichloride Chemical compound [Cl-].[Cl-].[Cl-].[K+].[Pt+2] QPINXQCQOKBINJ-UHFFFAOYSA-K 0.000 description 1
239000000843 powder Substances 0.000 description 1
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
239000002994 raw material Substances 0.000 description 1
238000010992 reflux Methods 0.000 description 1
229910052702 rhenium Inorganic materials 0.000 description 1
WUAPFZMCVAUBPE-UHFFFAOYSA-N rhenium atom Chemical compound [Re] WUAPFZMCVAUBPE-UHFFFAOYSA-N 0.000 description 1
229910052703 rhodium Inorganic materials 0.000 description 1
239000010948 rhodium Substances 0.000 description 1
MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical compound [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 description 1
229910052707 ruthenium Inorganic materials 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
239000000377 silicon dioxide Substances 0.000 description 1
238000003756 stirring Methods 0.000 description 1
150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
229920006337 unsaturated polyester resin Polymers 0.000 description 1
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1

Landscapes

Reinforced Plastic Materials (AREA)
Compositions Of Macromolecular Compounds (AREA)

JP12280178A 1978-10-05 1978-10-05 Organo-silane compound Granted JPS5549387A (en)

Priority Applications (1)

Application Number	Priority Date	Filing Date	Title
JP12280178A JPS5549387A (en)	1978-10-05	1978-10-05	Organo-silane compound

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
JP12280178A JPS5549387A (en)	1978-10-05	1978-10-05	Organo-silane compound

Publications (2)

Publication Number	Publication Date
JPS5549387A JPS5549387A (en)	1980-04-09
JPS6138197B2 true JPS6138197B2 (da)	1986-08-28

Family

ID=14844966

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP12280178A Granted JPS5549387A (en)	1978-10-05	1978-10-05	Organo-silane compound

Country Status (1)

Country	Link
JP (1)	JPS5549387A (da)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US11003227B2 (en)	2015-06-03	2021-05-11	Mitsubishi Electric Corporation	Liquid-type cooling apparatus and manufacturing method for heat radiation fin in liquid-type cooling apparatus

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JP6087499B2 (ja) *	2011-10-18	2017-03-01	信越化学工業株式会社	熱伝導性シリコーン組成物

1978
- 1978-10-05 JP JP12280178A patent/JPS5549387A/ja active Granted

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US11003227B2 (en)	2015-06-03	2021-05-11	Mitsubishi Electric Corporation	Liquid-type cooling apparatus and manufacturing method for heat radiation fin in liquid-type cooling apparatus

Also Published As

Publication number	Publication date
JPS5549387A (en)	1980-04-09

Publication	Publication Date	Title
EP0403706A2 (en)	1990-12-27	Process for preparing amino-propyl silanes
JP5115729B2 (ja)	2013-01-09	トリアルキルシリル基で保護されたアセト酢酸エステル基含有有機ケイ素化合物及びその製造方法
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CA2043383C (en)	2000-02-15	Sterically hindered aminohydrocarbyl silanes and process of preparation
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JPS6138197B2 (da)	1986-08-28
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JP2010013653A (ja)	2010-01-21	アルコール性水酸基を有する有機ケイ素樹脂及びその製造方法
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JP2003082102A (ja)	2003-03-19	オルガノオキシ基またはヒドロキシル基を有するシロキサンの製造方法
JPH04124189A (ja)	1992-04-24	有機ケイ素化合物の製造方法
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JP3622002B2 (ja)	2005-02-23	ホルムオキシシランの製造方法
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JPH0334988A (ja)	1991-02-14	アルコキシ基含有シロキサン化合物
JPH0459783A (ja)	1992-02-26	含フッ素有機ケイ素化合物
CN108586512A (zh)	2018-09-28	一种新型乙烯基硅基化合物的制备方法
JP4081572B2 (ja)	2008-04-30	水酸基を有する化合物のシリル化方法
JP3801391B2 (ja)	2006-07-26	４−ビニル−１−シクロヘキセンのヒドロシリル化方法
US5113000A (en)	1992-05-12	Organosilicon compound and acryl compound
JPH085903B2 (ja)	1996-01-24	エポキシ基含有アルコキシシロキサン及びその製造方法
JP2000086674A (ja)	2000-03-28	含ケイ素化合物および含ケイ素ポリマーの製造方法

JPS6138197B2 - - Google Patents

Info

Links

Landscapes

Priority Applications (1)

Applications Claiming Priority (1)

Publications (2)

Family

ID=14844966

Family Applications (1)

Country Status (1)

Cited By (1)

Families Citing this family (1)

Cited By (1)

Also Published As

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