KR920701103A - 개선된 비닐에테르 제조방법 - Google Patents
개선된 비닐에테르 제조방법Info
- Publication number
- KR920701103A KR920701103A KR1019910700729A KR910700729A KR920701103A KR 920701103 A KR920701103 A KR 920701103A KR 1019910700729 A KR1019910700729 A KR 1019910700729A KR 910700729 A KR910700729 A KR 910700729A KR 920701103 A KR920701103 A KR 920701103A
- Authority
- KR
- South Korea
- Prior art keywords
- group
- titanium
- metal
- reducing agent
- aryl
- Prior art date
Links
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical compound C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 title claims 3
- 238000004519 manufacturing process Methods 0.000 title 1
- 238000000034 method Methods 0.000 claims 16
- 125000003118 aryl group Chemical group 0.000 claims 6
- 150000001412 amines Chemical class 0.000 claims 5
- 239000003638 chemical reducing agent Substances 0.000 claims 5
- 229910052751 metal Inorganic materials 0.000 claims 5
- 239000002184 metal Substances 0.000 claims 5
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical group C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 claims 4
- 150000001875 compounds Chemical class 0.000 claims 4
- -1 ester compound Chemical class 0.000 claims 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 4
- 239000003960 organic solvent Substances 0.000 claims 4
- 150000003608 titanium Chemical class 0.000 claims 4
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical group CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 claims 3
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims 3
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims 3
- 229910052725 zinc Inorganic materials 0.000 claims 3
- 239000011701 zinc Substances 0.000 claims 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 2
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims 2
- 125000000217 alkyl group Chemical group 0.000 claims 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 2
- 125000004432 carbon atom Chemical group C* 0.000 claims 2
- 229910052760 oxygen Inorganic materials 0.000 claims 2
- 239000001301 oxygen Substances 0.000 claims 2
- 125000003367 polycyclic group Chemical group 0.000 claims 2
- 125000006239 protecting group Chemical group 0.000 claims 2
- 125000001424 substituent group Chemical group 0.000 claims 2
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 claims 2
- 239000010936 titanium Substances 0.000 claims 2
- 229910052719 titanium Inorganic materials 0.000 claims 2
- XJDNKRIXUMDJCW-UHFFFAOYSA-J titanium tetrachloride Chemical compound Cl[Ti](Cl)(Cl)Cl XJDNKRIXUMDJCW-UHFFFAOYSA-J 0.000 claims 2
- YONPGGFAJWQGJC-UHFFFAOYSA-K titanium(iii) chloride Chemical group Cl[Ti](Cl)Cl YONPGGFAJWQGJC-UHFFFAOYSA-K 0.000 claims 2
- 125000005389 trialkylsiloxy group Chemical group 0.000 claims 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 1
- 229910019142 PO4 Inorganic materials 0.000 claims 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims 1
- 125000003710 aryl alkyl group Chemical group 0.000 claims 1
- 125000005841 biaryl group Chemical group 0.000 claims 1
- 229910052799 carbon Inorganic materials 0.000 claims 1
- 150000001805 chlorine compounds Chemical group 0.000 claims 1
- 229910052736 halogen Inorganic materials 0.000 claims 1
- 150000002367 halogens Chemical class 0.000 claims 1
- 229910052757 nitrogen Inorganic materials 0.000 claims 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims 1
- 125000000962 organic group Chemical group 0.000 claims 1
- 150000003901 oxalic acid esters Chemical class 0.000 claims 1
- 235000021317 phosphate Nutrition 0.000 claims 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 claims 1
- 229910052698 phosphorus Inorganic materials 0.000 claims 1
- 239000011574 phosphorus Substances 0.000 claims 1
- 239000011833 salt mixture Substances 0.000 claims 1
- 150000003839 salts Chemical class 0.000 claims 1
- 125000004469 siloxy group Chemical group [SiH3]O* 0.000 claims 1
- 229910052717 sulfur Inorganic materials 0.000 claims 1
- 239000011593 sulfur Substances 0.000 claims 1
- 125000005259 triarylamine group Chemical group 0.000 claims 1
Classifications
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- A—HUMAN NECESSITIES
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- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L2/00—Methods or apparatus for disinfecting or sterilising materials or objects other than foodstuffs or contact lenses; Accessories therefor
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- C07C41/05—Preparation of ethers by addition of compounds to unsaturated compounds
- C07C41/06—Preparation of ethers by addition of compounds to unsaturated compounds by addition of organic compounds only
- C07C41/08—Preparation of ethers by addition of compounds to unsaturated compounds by addition of organic compounds only to carbon-to-carbon triple bonds
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- A61L2/00—Methods or apparatus for disinfecting or sterilising materials or objects other than foodstuffs or contact lenses; Accessories therefor
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Abstract
내용 없음
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
Claims (17)
- 유기용매속에서 다음 구조식(Ⅱ)으로 표현되는 카르보닐 함유 화합물을 역시 다음 구조식(Ⅲ)의 에스테르 화합물과 반응시켜서 아연금속, 티타늄염과 아민염기 존재하에 다음 구조식(Ⅰ)의 화합물을 제조하는 방법.여기서 A와 R은 수동적 유기그룹이고 ArOY는 히드록시기와 또한 P가 보호기일때 OP중에서 선택된 치환물인 OY로 치환된 아릴고리를 갖춘 아릴기이다.
- 제1항에 있어서, 금속형 환원제는 아연인 것을 특징으로 하는 방법.
- 제2항에 있어서, 티타늄은 3염화티타늄과 4염화티타늄 중에서 선택하는 것으로된 방법.
- 제3항에 있어서, 아민염기는 트리에릴아민이고 유기용매는 테트라히드로퓨란인 것으로된 방법.
- 제1항에 있어서, OY를 트리알킬실리옥시, 디알킬아릴 실리옥시, 디아릴알킬실리옥시와 트리아릴실리옥시 중에서 선택하여된 방법.
- 제1항에 있어서, OY가 히드록실기인 것으로된 방법.
- 유기용매속에서 다음구조식(Ⅴ)으로 표현되는 카르보닐 함유 화합물을 역시 다음 구조식(Ⅵ)의 에스테르 화합물과 반응시켜서 금속형 환원제, 티타늄금속염 또한 아민염기 존재하에 다음 구조식(Ⅳ)의 비닐에테르를 제조하는 방법에 대한 것이다.여기에 R1은 1내지 20 탄소원자를 함유한 알킬, 아릴 또한 아랄킬이고 때로는 산소, 황, 질소, 인 및 할로겐을 함유하며, R2는 아릴, 비아릴 및 치환 혹은 비치환된 융해고리 다중고리형 아릴기중에서 선택된 것이고 또한 R1과 R2는 탄소, 산소 및 질소함유기중에서 선택된 성분으로 함께 결합될 수 있고, R3C-는 6내지 30탄소원자를 함유한 다중고리형 알킬기중에서 선택하고, OY는 히드록시기와 또한 P가 보호기일때의 OP기중에서 선택된 치환물이다.
- 제7항에 있어서, 금속형 환원제는 아연인 것을 특징으로 하는 방법.
- 제8항에 있어서, 티타늄염은 3염화티타늄과 4염화티타늄중에서 선택하는 것으로된 방법.
- 제9항에 있어서, 아민염기는 트리에틸아민과 유기용매는 테트라히드로퓨란인 것으로된 방법.
- 제7항에 있어서, OY를 트리알킬실리옥시, 디알킬 아릴실리옥시, 디아릴알킬실리옥시와 트리아릴실리옥시중에서 선택하여된 방법.
- 제7항에 있어서, OY는 히드록실기인 것으로된 방법.
- 제7항에 있어서, 비닐에테르속의 Y가 OX기를 제공하는 또다른기로 대체되는 것을 특징으로 하는 방법.
- 제7항에 있어서, OX기를 무기 산소산염, 인산염, 산소-피라노시드, 아릴 및 알킬 카르복실 에스테르중에서 선택하여된 방법.
- 제1항에 있어서, 카르보닐 함유 화합물과 에스테르 화합물의 반응에 앞서서 금속형 환원제와 티타늄염 혼합물에 아민을 서서히 첨가하는 것으로된 방법.
- 제15항에 있어서, 티타늄염이 염화물인 것으로된 방법.
- 제16항에 있어서, 금속형 환원제는 미세하게 분쇄한 것인 방법.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US450459 | 1989-12-14 | ||
US450,459 | 1989-12-14 | ||
US07/450,459 US4983779A (en) | 1986-07-17 | 1989-12-14 | Process for the preparation of vinyl ethers |
PCT/US1990/007372 WO1991009002A1 (en) | 1989-12-14 | 1990-12-12 | Process for the preparation of vinyl ethers |
Publications (2)
Publication Number | Publication Date |
---|---|
KR920701103A true KR920701103A (ko) | 1992-08-11 |
KR950001678B1 KR950001678B1 (ko) | 1995-02-28 |
Family
ID=23788187
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1019910700729A KR950001678B1 (ko) | 1989-12-14 | 1990-12-12 | 개선된 비닐에테르 제조방법 |
Country Status (13)
Country | Link |
---|---|
US (1) | US4983779A (ko) |
EP (1) | EP0458965B1 (ko) |
JP (2) | JPH0825941B2 (ko) |
KR (1) | KR950001678B1 (ko) |
CN (1) | CN1020893C (ko) |
AT (1) | ATE128110T1 (ko) |
AU (1) | AU637194B2 (ko) |
CA (1) | CA2045553C (ko) |
DE (1) | DE69022582T2 (ko) |
DK (1) | DK0458965T3 (ko) |
ES (1) | ES2080296T3 (ko) |
GR (1) | GR3018174T3 (ko) |
WO (1) | WO1991009002A1 (ko) |
Families Citing this family (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0731201B2 (ja) | 1987-12-31 | 1995-04-10 | トロピックス・インコーポレーテッド | 化学発光による測定法 |
US5582980A (en) * | 1989-07-17 | 1996-12-10 | Tropix, Inc. | Chemiluminescent 1,2-dioxetanes |
US6022964A (en) | 1989-07-17 | 2000-02-08 | Tropix, Inc. | Chemiluminescent 1,2-dioxetanes |
US5326882A (en) * | 1989-07-17 | 1994-07-05 | Tropix, Inc. | Chemiluminescent 3-(substituted Adamant-2'-Ylidene) 1,2-dioxetanes |
ATE174914T1 (de) * | 1990-08-30 | 1999-01-15 | Tropix Inc | Chemolumineszente 3-(substituierte adamant-2'- ylidene)1,2-dioxetane |
DE4210759A1 (de) * | 1992-04-01 | 1993-10-07 | Boehringer Mannheim Gmbh | Substituierte Thiazolin-Dioxetan-Substrate, Verfahren zur Herstellung und Verwendung |
AU1518195A (en) * | 1993-12-23 | 1995-07-10 | Tropix, Inc. | Chemiluminescent energy transfer assays |
US5773628A (en) * | 1994-11-14 | 1998-06-30 | Tropix, Inc. | 1,2-dioxetane compounds with haloalkoxy groups, methods preparation and use |
US5721370A (en) * | 1995-07-31 | 1998-02-24 | Lumigen Inc. | Water soluble tri-substituted 1,2-dioxetane compounds and assay compositions having increased storage stability |
CN101496917B (zh) | 2003-05-21 | 2013-07-31 | 株式会社Jms | 细胞培养的血清调制装置和血清调制方法及细胞培养方法 |
CN100525906C (zh) * | 2007-02-09 | 2009-08-12 | 上海华谊丙烯酸有限公司 | 缩醛气相分解催化剂及其制备方法 |
CN102030779A (zh) * | 2010-11-17 | 2011-04-27 | 云南瑞亘生物科技有限公司 | 一种免疫分析用化学发光物amppd的制备方法 |
CA3011328A1 (en) * | 2016-01-26 | 2017-08-03 | Ramot At Tel-Aviv University Ltd. | Chemiluminescent probes for diagnostics and in vivo imaging |
US11857674B2 (en) | 2016-05-18 | 2024-01-02 | Reoxcyn, Llc | Lubricant formulations |
US9474768B1 (en) * | 2016-05-18 | 2016-10-25 | Reoxcyn Discoveries Group, Inc. | Lubricant formulations |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4857652A (en) * | 1986-07-17 | 1989-08-15 | Board Of Governors Of Wayne State University | Chemiluminescent 1,2-dioxetane compounds |
-
1989
- 1989-12-14 US US07/450,459 patent/US4983779A/en not_active Expired - Lifetime
-
1990
- 1990-12-12 AU AU71833/91A patent/AU637194B2/en not_active Ceased
- 1990-12-12 WO PCT/US1990/007372 patent/WO1991009002A1/en active IP Right Grant
- 1990-12-12 AT AT91903105T patent/ATE128110T1/de not_active IP Right Cessation
- 1990-12-12 DE DE69022582T patent/DE69022582T2/de not_active Expired - Fee Related
- 1990-12-12 KR KR1019910700729A patent/KR950001678B1/ko not_active IP Right Cessation
- 1990-12-12 EP EP91903105A patent/EP0458965B1/en not_active Expired - Lifetime
- 1990-12-12 JP JP3503256A patent/JPH0825941B2/ja not_active Expired - Lifetime
- 1990-12-12 JP JP91503256A patent/JPH04505458A/ja not_active Withdrawn
- 1990-12-12 DK DK91903105.4T patent/DK0458965T3/da active
- 1990-12-12 ES ES91903105T patent/ES2080296T3/es not_active Expired - Lifetime
- 1990-12-12 CA CA002045553A patent/CA2045553C/en not_active Expired - Fee Related
- 1990-12-14 CN CN90106055A patent/CN1020893C/zh not_active Expired - Fee Related
-
1995
- 1995-11-22 GR GR950403293T patent/GR3018174T3/el unknown
Also Published As
Publication number | Publication date |
---|---|
EP0458965A4 (en) | 1993-07-28 |
EP0458965B1 (en) | 1995-09-20 |
US4983779A (en) | 1991-01-08 |
ES2080296T3 (es) | 1996-02-01 |
CA2045553C (en) | 1999-04-13 |
DE69022582T2 (de) | 1996-03-07 |
CN1020893C (zh) | 1993-05-26 |
JPH03504815A (ja) | 1991-10-24 |
JPH0825941B2 (ja) | 1996-03-13 |
WO1991009002A1 (en) | 1991-06-27 |
CA2045553A1 (en) | 1991-06-15 |
EP0458965A1 (en) | 1991-12-04 |
DK0458965T3 (da) | 1996-01-15 |
JPH04505458A (ja) | 1992-09-24 |
AU637194B2 (en) | 1993-05-20 |
ATE128110T1 (de) | 1995-10-15 |
DE69022582D1 (de) | 1995-10-26 |
CN1052478A (zh) | 1991-06-26 |
AU7183391A (en) | 1991-07-18 |
GR3018174T3 (en) | 1996-02-29 |
KR950001678B1 (ko) | 1995-02-28 |
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