KR850005448A - 펜옥시 프로피오닐옥시 알칸 포스포네이트의 제조방법 - Google Patents
펜옥시 프로피오닐옥시 알칸 포스포네이트의 제조방법 Download PDFInfo
- Publication number
- KR850005448A KR850005448A KR1019850000471A KR850000471A KR850005448A KR 850005448 A KR850005448 A KR 850005448A KR 1019850000471 A KR1019850000471 A KR 1019850000471A KR 850000471 A KR850000471 A KR 850000471A KR 850005448 A KR850005448 A KR 850005448A
- Authority
- KR
- South Korea
- Prior art keywords
- phosphonate
- formula
- optionally
- phenoxy
- alkyl
- Prior art date
Links
- UEZVMMHDMIWARA-UHFFFAOYSA-M phosphonate Chemical compound [O-]P(=O)=O UEZVMMHDMIWARA-UHFFFAOYSA-M 0.000 title claims 8
- -1 phenoxy propionyloxy Chemical group 0.000 title claims 6
- 238000000034 method Methods 0.000 title claims 5
- 150000001335 aliphatic alkanes Chemical class 0.000 title claims 4
- 239000002253 acid Substances 0.000 claims 3
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims 3
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims 2
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 2
- 239000011230 binding agent Substances 0.000 claims 2
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims 2
- 229910052794 bromium Inorganic materials 0.000 claims 2
- 125000004432 carbon atom Chemical group C* 0.000 claims 2
- 239000003795 chemical substances by application Substances 0.000 claims 2
- 229910052801 chlorine Inorganic materials 0.000 claims 2
- 239000000460 chlorine Substances 0.000 claims 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 2
- 230000002087 whitening effect Effects 0.000 claims 2
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims 1
- NADUNELKTNMTOZ-UHFFFAOYSA-N 2-[4-(3,5-dichloropyridin-2-yl)oxyphenoxy]propanoyl chloride Chemical compound C1=CC(OC(C)C(Cl)=O)=CC=C1OC1=NC=C(Cl)C=C1Cl NADUNELKTNMTOZ-UHFFFAOYSA-N 0.000 claims 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims 1
- 125000000217 alkyl group Chemical group 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 claims 1
- 239000003085 diluting agent Substances 0.000 claims 1
- 229910052731 fluorine Inorganic materials 0.000 claims 1
- 239000011737 fluorine Substances 0.000 claims 1
- 125000004438 haloalkoxy group Chemical group 0.000 claims 1
- 125000001188 haloalkyl group Chemical group 0.000 claims 1
- 229910052736 halogen Inorganic materials 0.000 claims 1
- 150000002367 halogens Chemical group 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 1
- 125000004076 pyridyl group Chemical group 0.000 claims 1
- 125000000547 substituted alkyl group Chemical group 0.000 claims 1
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
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/38—Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)]
-
- 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
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/38—Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)]
- C07F9/40—Esters thereof
- C07F9/4003—Esters thereof the acid moiety containing a substituent or a structure which is considered as characteristic
- C07F9/4006—Esters of acyclic acids which can have further substituents on alkyl
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N57/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
- A01N57/18—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-carbon bonds
- A01N57/24—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-carbon bonds containing heterocyclic radicals
-
- 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
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/38—Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)]
- C07F9/40—Esters thereof
-
- 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
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/553—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having one nitrogen atom as the only ring hetero atom
- C07F9/576—Six-membered rings
- C07F9/58—Pyridine rings
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Biochemistry (AREA)
- Molecular Biology (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Plant Pathology (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
내용 없음
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
Claims (5)
- 구조식 (Ⅱ)의 2-[4-(3,5-디클로로피리딘-2-일옥시)-펜옥시]-프로피오닐 클로라이드를, 경우에 따라 산 수용체 존재하 및 경우에 따라 희색제의 존재하에서, 일반식(Ⅲ)의 하이드록시 알칸 포스포네이트와 반응시키거나; 일반식(Ⅲ)의 하이드록시 알칸 포스포네이트를, 경우에 따라 산결합제 존재하 및 경우에 따라 희색제의 존재하에서, 일반식(Ⅳ)의 할로게노 프로피오닐 할라이드와 반응시키고, 생성된 일반식(Ⅴ)의 프로피오닐옥시알칸 포스포네이트를, 경우에 따라 산결합재 존재하 및 경우에 따라 희색제의 존재하에서, 구조식(Ⅵ)의 4-(3,5-디클로로피리딘-2-일옥시)페놀과 반응시킴을 특징으로 하여, 일반식(Ⅰ)의 펜옥시프로피오닐옥시 알칸 포스포네이트를 제조하는 방법.(Ⅵ)상기식에서 R은 임의 치환된 알킬이고; A는 임의 치환된 알칸디일이며; Hal및 Hal'는 서로 독립적으로 염소 또는 브롬을 나타낸다.
- 제1항에 있어서, R은 할로겐에 의해 임의 치환된, 탄소수 1내지 6의 알킬이고; A는 탄소수 1내지 4의 알킬, 피리딜 및/또는, 불소, 염소, 브롬, 니트로, 탄소수 1내지 4의 알킬, 탄소수 1내지 4의 알콕시, 탄소수 1내지 4의 할로게노알킬, 탄소수 1내지 4의 할로게노 알콕시, 펜옥시 및/또는 메틸렌 디옥시에 의해 일치환 내지 삼치환될 수 있는 페닐에 의해 치환될 수 있는, 탄소수 1내지 6의 알칸디일을 나타내는 일반식(Ⅰ)의 펜옥시프로피오닐옥시 알칸 포스포 네이트를 제조하는 방법.
- 제1항에 있어서, 다음 구조식의 펜옥시프로피오닐옥시알칸 포스포네이트를 제조하는 방법.
- 제1항에 있어서, 다음 구조식의 펜옥시 프로피오닐옥시알칸 포스포네이트를 제조하는 방법.
- 제1항에 있어서, 다음 구조식의 펜옥시 프로피오닐옥시알칸 포스포네이트를 제조하는 방법.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE3402982.6 | 1984-01-28 | ||
DE19843402982 DE3402982A1 (de) | 1984-01-28 | 1984-01-28 | Phenoxypropionyloxyalkanphosphonsaeureester |
Publications (1)
Publication Number | Publication Date |
---|---|
KR850005448A true KR850005448A (ko) | 1985-08-26 |
Family
ID=6226177
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1019850000471A KR850005448A (ko) | 1984-01-28 | 1985-01-25 | 펜옥시 프로피오닐옥시 알칸 포스포네이트의 제조방법 |
Country Status (11)
Country | Link |
---|---|
US (2) | US4670040A (ko) |
EP (1) | EP0151945A1 (ko) |
JP (1) | JPS60163891A (ko) |
KR (1) | KR850005448A (ko) |
AU (1) | AU566099B2 (ko) |
BR (1) | BR8500334A (ko) |
CA (1) | CA1209147A (ko) |
DE (1) | DE3402982A1 (ko) |
DK (1) | DK36485A (ko) |
IL (1) | IL74164A0 (ko) |
ZA (1) | ZA85612B (ko) |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3402982A1 (de) * | 1984-01-28 | 1985-08-01 | Bayer Ag, 5090 Leverkusen | Phenoxypropionyloxyalkanphosphonsaeureester |
EP0200677B1 (de) * | 1985-04-01 | 1991-04-03 | Ciba-Geigy Ag | 3-Fluorpyridyl-2-oxy-phenoxy-Derivate mit herbizider Wirkung |
US5236481A (en) * | 1992-02-21 | 1993-08-17 | Corning Incorporated | Method of doping porous glass preforms |
US7233899B2 (en) * | 2001-03-12 | 2007-06-19 | Fain Vitaliy S | Speech recognition system using normalized voiced segment spectrogram analysis |
CN107176950B (zh) * | 2017-06-01 | 2019-12-31 | 赣州市正畅塑胶有限公司 | 一种芳氧苯氧基丙酸酯类化合物及其制备方法与应用 |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4322241A (en) * | 1979-08-07 | 1982-03-30 | Ciba-Geigy Corporation | Pyridyl-2-oxyphenyloxime derivatives, and their use as herbicides |
US4326880A (en) * | 1979-08-14 | 1982-04-27 | Ciba-Geigy Corporation | Derivatives of 5-(pyridyl-2-oxy)-2-nitrobenzoic acid, and herbicidal compositions containing them, and herbicidal methods for using same |
JPS5832890A (ja) * | 1981-08-21 | 1983-02-25 | Sumitomo Chem Co Ltd | ホスホン酸エステル誘導体、その製造方法およびそれを有効成分とする除草剤 |
US4518416A (en) * | 1982-06-04 | 1985-05-21 | Bayer Aktiengesellschaft | Certain trimethyl silyl-lower-alkyl esters of pyridyloxy-phenoxy-lower alkanoic acids, compositions containing same and herbicidal method of use |
CA1246571A (en) * | 1983-04-06 | 1988-12-13 | Georg E. Frater | Propionic acid esters |
DE3402982A1 (de) * | 1984-01-28 | 1985-08-01 | Bayer Ag, 5090 Leverkusen | Phenoxypropionyloxyalkanphosphonsaeureester |
-
1984
- 1984-01-28 DE DE19843402982 patent/DE3402982A1/de not_active Withdrawn
-
1985
- 1985-01-16 EP EP85100380A patent/EP0151945A1/de not_active Withdrawn
- 1985-01-21 AU AU37950/85A patent/AU566099B2/en not_active Ceased
- 1985-01-24 US US06/694,548 patent/US4670040A/en not_active Expired - Fee Related
- 1985-01-24 JP JP60009999A patent/JPS60163891A/ja active Pending
- 1985-01-25 KR KR1019850000471A patent/KR850005448A/ko not_active Application Discontinuation
- 1985-01-25 BR BR8500334A patent/BR8500334A/pt unknown
- 1985-01-25 ZA ZA85612A patent/ZA85612B/xx unknown
- 1985-01-25 DK DK36485A patent/DK36485A/da not_active Application Discontinuation
- 1985-01-25 CA CA000472873A patent/CA1209147A/en not_active Expired
- 1985-01-25 IL IL74164A patent/IL74164A0/xx unknown
-
1987
- 1987-01-07 US US07/001,117 patent/US4787929A/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
ZA85612B (en) | 1985-09-25 |
AU566099B2 (en) | 1987-10-08 |
CA1209147A (en) | 1986-08-05 |
US4787929A (en) | 1988-11-29 |
DE3402982A1 (de) | 1985-08-01 |
DK36485A (da) | 1985-07-29 |
AU3795085A (en) | 1985-08-01 |
EP0151945A1 (de) | 1985-08-21 |
US4670040A (en) | 1987-06-02 |
IL74164A0 (en) | 1985-04-30 |
DK36485D0 (da) | 1985-01-25 |
BR8500334A (pt) | 1985-09-03 |
JPS60163891A (ja) | 1985-08-26 |
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Legal Events
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WITN | Application deemed withdrawn, e.g. because no request for examination was filed or no examination fee was paid |