KR890000557A - N-(폴리옥시알킬)-n-(알킬)아민 - Google Patents
N-(폴리옥시알킬)-n-(알킬)아민 Download PDFInfo
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- KR890000557A KR890000557A KR1019880007879A KR880007879A KR890000557A KR 890000557 A KR890000557 A KR 890000557A KR 1019880007879 A KR1019880007879 A KR 1019880007879A KR 880007879 A KR880007879 A KR 880007879A KR 890000557 A KR890000557 A KR 890000557A
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G73/00—Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups C08G12/00 - C08G71/00
- C08G73/02—Polyamines
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/02—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
- C08G65/32—Polymers modified by chemical after-treatment
- C08G65/329—Polymers modified by chemical after-treatment with organic compounds
- C08G65/333—Polymers modified by chemical after-treatment with organic compounds containing nitrogen
- C08G65/33303—Polymers modified by chemical after-treatment with organic compounds containing nitrogen containing amino group
- C08G65/33306—Polymers modified by chemical after-treatment with organic compounds containing nitrogen containing amino group acyclic
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
- C08G18/48—Polyethers
- C08G18/50—Polyethers having heteroatoms other than oxygen
- C08G18/5021—Polyethers having heteroatoms other than oxygen having nitrogen
- C08G18/5024—Polyethers having heteroatoms other than oxygen having nitrogen containing primary and/or secondary amino groups
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/02—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
- C08G65/32—Polymers modified by chemical after-treatment
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/02—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
- C08G65/32—Polymers modified by chemical after-treatment
- C08G65/321—Polymers modified by chemical after-treatment with inorganic compounds
- C08G65/322—Polymers modified by chemical after-treatment with inorganic compounds containing hydrogen
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- Chemical & Material Sciences (AREA)
- Polymers & Plastics (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Organic Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Inorganic Chemistry (AREA)
- Polyurethanes Or Polyureas (AREA)
- Polyethers (AREA)
- Lubricants (AREA)
- Pyridine Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
내용 없음
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
Claims (20)
- 하기 일반식의 N-(폴리옥시알킬)-N-(알킬)아민.R[H](hz)[(P)p(S)s(T)t]z←(hz8상기식에서, R은 쩨레비티노프(Zerewitinoff)활성수소원자를 함유하는 화합물을 기본으로 하는 개시제 라디칼이고; H는 일반식의 그룹이고; P는 일반식의 그룹이고; S는 일반식 의 그룹이고; T는 일반식 의 그룹이고; a는 0 내지 175이고; b는 0내지 175이고; c는 0 내지 30이고, n은 1 내지 3이고; a+b+c의 합은 n이 1일때에 2이상이어야 하고; R′은 2 내지 18개의 탄소원자를 함유하는 알킬 그룹이고; R″은 수소이거나, 18개이하의 탄소원자를 함유하는 알킬그룹이고; R″′ 및 R″″은 독립적으로 2 내지 12개의 탄소원자를 함유하는 알킬그룹이고; h는 0 내지 0.7이고; p는 0 내지 0.5미만이고; s는 0.5 내지 1.0이고; t는 0 내지 0.15이고; z는 개시제상에 존재하는 째레비티노프 활성 수소의 수로부터 유도된 정수인데, 단 Z가 2이고 a와 c가 0이면, b는 22보다 커야 한다.
- 제1항에 있어서, R이 2 내지 6개의 탄소원자르 함유하고, a가 0 내지 5O이고, b가 20 내지 115이고, c가 0 내지 15이고, R′가 2개의 탄소원자를 함유하는 알킬 그룹이고, R″′이 2 내지 6개의 탄소원자를 함유하고, Z가 2 내지 6인 N-(폴리옥시알킬)-N-(알킬)아민.
- 제2항에 있어서, R이 3 내지 6개의 탄소원자를 함유하고, a가 0 내지 90이고, b가 25내지 98이고, c가 0 내지 2이고, R″′이 이소프로필그룹이고, Z가 3 내지 6인 N-(폴리오기알킬)-N-(알킬)아민.
- 제1항에 있어서, R의 분자량이 18 내지 400인 N-(폴리옥시알킬)-N-(알킬)아민.
- 제3항에 있어서, R이인 N-(폴리옥시알킬)-N-(알킬)아민.
- 당량이 약1,000 내지 10,000인 학 일반식의 N-(폴리옥시알킬)-N-(알킬)아민.R[H](hz)[(P)p(S)s(T)t]z←(hz)상기식에서, R은 째레비티노프 활성 수소원자를 함유하는 화합물을 기본으로 하는 개시제 라디칼이고; H는 일반식의 그룹이고, P는 일반식의 그룹이고; S는 일반식 의 그룹이고; T는 일반식 의 그룹이고; a는 0 내지 175이고; b는 0내지 175이고; c는 0 내지 30이고, n은 1 내지 3이고; a+b+c의 합은 n이 1일때에 2이상이고; R′은 2 내지 18개의 탄소원자를 함유하는 알킬 그룹이고; R″은 수소이거나, 18개이하의 탄소원자를 함유하는 알킬그룹이고; R″′ 및 R″″은 독립적으로 2 내지 12개의 탄소원자를 함유하는 알킬그룹이고; h는 0 내지 0.3이고; p는 0 내지 0.4이고; s는 0.7 내지 1.0이고; t는 0 내지 0.05이고; z는 2 내지 6인데, 단 z가 2이고 a+c가 0이면, b는 22보다 커야 한다.
- 제6항에 있어서, R이 2 내지 6개의 탄소원자를 함유하고, a가 0 내지 150이고, b가 20 내지 115이고, c가 0 내지 15이고, R'이 2개의 탄소원자를 함유하는 알킬그루이고, R″′이 2 내지 6개의 탄소원자를 함유하고, Z가 2 내지 6인 N-(폴리옥시알킬)-N-(알킬)아민.
- 제7항에 있어서, R이 3 내지 6개의 탄소원자를 함유하고, a가 0 내지 90이고, b가 25 내지 98이고, c가 0 내지 2이고, R″′이 이소프로필그룹이고, Z가 3 내지 6인 N-(폴리옥시알킬)-N-(알킬)아민.
- 제6항에 있어서, R의 분자량이 18 내지 400인 N-(폴리옥시알킬)-N-(알킬)아민.
- 제8항에 있어서, R이인 N-(폴리옥시알킬)-N-(알킬)아민.
- 하기 일반식의 N-(폴리옥시알킬)-N-(알킬)아민.R[H](hz)[(P)p(S)s(T)t]z←(hz)상기식에서, R은 째레비티노프 활성수소원자를 함유하는 화합물을 기본으로 하는 개시제 라디칼이고; H는 일반식 하는 개시제 라디칼이고; H는 일반식의 그룹이고, P는 일반식 의 그룹이고; S는 일반식 의 그룹이고; T는 일반식 의 그룹이고; a는 0 내지 175이고; b는 0내지 175이고; c는 0 내지 30이고; n은 1 내지 3이고; a+b+c의 합은 n이 1일때에 2이상이고; R′은 2 내지 18개의 탄소원자를 함유하는 알킬그룹이고; R″은 수소이거나 18개이하의 탄소원자를 함유하는 알킬그룹이고; R″′ 및 R″″은 독립적으로 2 내지 12개의 탄소원자를 함유하는 알킬그룹이고; h는 0 내지 0.15이고; p는 0 내지 0.4이고; s는 0.7 내지 1.0이고; t는 0 내지 0.05이고; z는 3 내지 6이다.
- 제11항에 있어서, R이 2 내지 6개의 탄소원자를 함유하고, a가 0 내지 150이고, b가 20 내지 115이고, c가 0 내지 15이고, R′이 2개의 탄소원자를 함유하는 알킬 그룹이고, R″′이 2 내지 6개의 탄소원자를 함유하는 N-(폴리옥시알킬)-N-(알킬)아민.
- 제12항에 있어서, R이 3 내지 6개의 탄소원자를 함유하고, a가 0 내지 90이고, b가 25 내지 98이고, c가 0 내지 2이고, R″′이 이소프로필그룹인 N-(폴리옥시알킬)N-(알킬아민)
- 제11항에 있어서, R의 분자량이 18 내지 400인 N-(폴리옥시알킬)-N-(알킬)아민.
- 제14항에 있어서, R이인 N-(폴리옥시알킬)-N-(알킬)아민.
- 당량이 약1,000 내지 10,000인 하기 일반식의 N-(폴리옥시알킬)-N-(알킬)아민.R[H](hz)[(P)p(S)s(T)t]z←(hz상기식에서, R은 째레비티노프 활성수소원자를 함유하는 화합물을 기본으로 하는 개시제 라디칼이고; H는 일반식의 그룹이고, P는 일반식의 그룹이고; S는 일반식 의 그룹이고; T는 일반식 의 그룹이고; a는 0 내지 175이고; b는 0내지 175이고; c는 0 내지 30이고; n은 1 내지 3이고; a+b+c의 합은 n이 1일때에 2이상이고; R′은 2 내지 18개의 탄소원자를 함유하는 알킬그룹이고; R″은 수소이거나, 18개이하의 탄소원자를 함유하는 알킬그룹이고; R′″은 2 내지 12개의 탄소원자를 함유하는 알킬 또는 아릴그룹이고; h는 0 내지 0.15이고; p는 0 내지 0.4이고; s는 0.7 내지 1.0이고; t는 0 내지 0.05이고; z는 3 내지 6이다.
- 제16항에 있어서, R이 3 내지 6개의 탄소원자를 함유하고, a가 0 내기 150이고, b가 20 내지 115이고, c가 0 내지 15이고, R′이 2개 탄소원자를 함유하는 알킬그룹이고, R″′이 2 내지 6개의 탄소원자를 함유하는 N-(폴리옥시알킬)-N-(알킬)아민.
- 제17항에 있어서, a가 0 내지 90이고, b가 25 내지 98이고, C가 0 내지 2이고, R′″이 이소프로필그룹인 N-(폴리옥시알킬)-N-(알킬)아민.
- 제16항에 있어서, R의 분자량이 18 내지 400인 N-(폴리옥시알킬)-N-(알킬)아민.
- 제19항에 있어서, R이인 N-(폴리옥시아킬)-N-(알킬)아민.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (6)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US6782287A | 1987-06-30 | 1987-06-30 | |
US067,822 | 1987-06-30 | ||
US67822 | 1987-06-30 | ||
US176217 | 1988-03-31 | ||
US07/176,217 US4902777A (en) | 1987-06-30 | 1988-03-31 | N-(polyoxyalkyl)-n-(alkyl)amines |
US176,217 | 1988-05-31 |
Publications (2)
Publication Number | Publication Date |
---|---|
KR890000557A true KR890000557A (ko) | 1989-03-15 |
KR930006049B1 KR930006049B1 (ko) | 1993-07-03 |
Family
ID=26748301
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1019880007879A KR930006049B1 (ko) | 1987-06-30 | 1988-06-29 | N-(폴리옥시알킬)-n-(알킬)아민 |
Country Status (8)
Country | Link |
---|---|
US (1) | US4902777A (ko) |
EP (1) | EP0297536B1 (ko) |
KR (1) | KR930006049B1 (ko) |
AT (1) | ATE156846T1 (ko) |
AU (1) | AU613928B2 (ko) |
BR (1) | BR8803208A (ko) |
CA (1) | CA1304414C (ko) |
DE (1) | DE3855994T2 (ko) |
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US4960942A (en) * | 1988-05-17 | 1990-10-02 | Union Carbide Chemicals And Plastics Company Inc. | Process for the manufacture of N-(polyoxyalkyl)-N-(alkyl)amines |
JP2795491B2 (ja) * | 1988-11-16 | 1998-09-10 | 三井化学株式会社 | 分子末端に2級アミノ基を有するポリオキシアルキレンポリアミンを製造する方法 |
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JP5039836B2 (ja) * | 2007-10-30 | 2012-10-03 | ソシエテ ド テクノロジー ミシュラン | ポリウレタン尿素系 |
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-
1988
- 1988-03-31 US US07/176,217 patent/US4902777A/en not_active Expired - Fee Related
- 1988-06-29 AT AT88110369T patent/ATE156846T1/de not_active IP Right Cessation
- 1988-06-29 DE DE3855994T patent/DE3855994T2/de not_active Expired - Fee Related
- 1988-06-29 BR BR888803208A patent/BR8803208A/pt not_active Application Discontinuation
- 1988-06-29 EP EP88110369A patent/EP0297536B1/en not_active Expired - Lifetime
- 1988-06-29 AU AU18543/88A patent/AU613928B2/en not_active Ceased
- 1988-06-29 CA CA000570791A patent/CA1304414C/en not_active Expired - Lifetime
- 1988-06-29 KR KR1019880007879A patent/KR930006049B1/ko not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
EP0297536A3 (en) | 1990-06-13 |
AU613928B2 (en) | 1991-08-15 |
DE3855994D1 (de) | 1997-09-18 |
US4902777A (en) | 1990-02-20 |
AU1854388A (en) | 1989-01-05 |
CA1304414C (en) | 1992-06-30 |
EP0297536B1 (en) | 1997-08-13 |
KR930006049B1 (ko) | 1993-07-03 |
ATE156846T1 (de) | 1997-08-15 |
DE3855994T2 (de) | 1997-12-18 |
EP0297536A2 (en) | 1989-01-04 |
BR8803208A (pt) | 1989-01-17 |
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