DD145748A5 - Verfahren zur herstellung von trifluormethylphenoxyphenoxycrotonsaeure-derivaten - Google Patents

Verfahren zur herstellung von trifluormethylphenoxyphenoxycrotonsaeure-derivaten Download PDF

Info

Publication number: DD145748A5
Authority: DD; German Democratic Republic
Prior art keywords: phenoxy; methyl; acid; crotonate; connection
Prior art date: 1978-02-14

Application number

DD21530878A

Other languages

German (de)

English (en)

Inventor

Kazuo Jikihara

Shigekazu Itoh

Shuichi Takayama

Koichi Sato

Ichiro Kimura

Isao Chiyomaru

Original Assignee

Kumiai Chemical Industry Co

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.)

1978-02-14

Filing date

1978-09-25

Publication date

1981-01-07

1978-09-25 Application filed by Kumiai Chemical Industry Co filed Critical Kumiai Chemical Industry Co

1981-01-07 Publication of DD145748A5 publication Critical patent/DD145748A5/de

Links

239000002253 acid Substances 0.000 title claims description 9
238000004519 manufacturing process Methods 0.000 title description 9
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 39
238000000034 method Methods 0.000 claims description 19
BIRWNTKNVDGIQD-CCEZHUSRSA-N FC(F)(F)C/C(=C(/C(=O)O)OC1=CC=CC=C1)/OC1=CC=CC=C1 Chemical class FC(F)(F)C/C(=C(/C(=O)O)OC1=CC=CC=C1)/OC1=CC=CC=C1 BIRWNTKNVDGIQD-CCEZHUSRSA-N 0.000 claims description 12
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 9
125000005843 halogen group Chemical group 0.000 claims description 8
125000003342 alkenyl group Chemical group 0.000 claims description 7
125000000217 alkyl group Chemical group 0.000 claims description 7
125000000304 alkynyl group Chemical group 0.000 claims description 7
125000000262 haloalkenyl group Chemical group 0.000 claims description 6
125000001188 haloalkyl group Chemical group 0.000 claims description 6
101150065749 Churc1 gene Proteins 0.000 claims description 3
GVNVAWHJIKLAGL-UHFFFAOYSA-N 2-(cyclohexen-1-yl)cyclohexan-1-one Chemical compound O=C1CCCCC1C1=CCCCC1 GVNVAWHJIKLAGL-UHFFFAOYSA-N 0.000 claims description 2
TYMVVQKMPXRTMP-UHFFFAOYSA-N 2-phenoxy-3-(trifluoromethyl)phenol Chemical class OC1=CC=CC(C(F)(F)F)=C1OC1=CC=CC=C1 TYMVVQKMPXRTMP-UHFFFAOYSA-N 0.000 claims description 2
102100038239 Protein Churchill Human genes 0.000 claims description 2
229910052739 hydrogen Inorganic materials 0.000 claims description 2
239000001257 hydrogen Substances 0.000 claims description 2
125000004185 ester group Chemical group 0.000 claims 2
101000588924 Anthopleura elegantissima Delta-actitoxin-Ael1a Proteins 0.000 claims 1
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims 1
239000012024 dehydrating agents‎ Substances 0.000 claims 1
150000004820 halides Chemical class 0.000 claims 1
150000001875 compounds Chemical class 0.000 description 61
125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 54
LDHQCZJRKDOVOX-NSCUHMNNSA-N crotonic acid Chemical compound C\C=C\C(O)=O LDHQCZJRKDOVOX-NSCUHMNNSA-N 0.000 description 52
-1 Halogcnalkyl- Chemical group 0.000 description 39
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230000002363 herbicidal effect Effects 0.000 description 28
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XXROGKLTLUQVRX-UHFFFAOYSA-N allyl alcohol Chemical compound OCC=C XXROGKLTLUQVRX-UHFFFAOYSA-N 0.000 description 6
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239000000460 chlorine Substances 0.000 description 5
230000000052 comparative effect Effects 0.000 description 5
239000008187 granular material Substances 0.000 description 5
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 5
229910052757 nitrogen Inorganic materials 0.000 description 5
239000012429 reaction media Substances 0.000 description 5
QDRKDTQENPPHOJ-UHFFFAOYSA-N sodium ethoxide Chemical compound [Na+].CC[O-] QDRKDTQENPPHOJ-UHFFFAOYSA-N 0.000 description 5
LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 5
241000189415 Alopecurus aequalis Species 0.000 description 4
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ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 4
HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 4
235000017896 Digitaria Nutrition 0.000 description 4
241001303487 Digitaria <clam> Species 0.000 description 4
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KKEYFWRCBNTPAC-UHFFFAOYSA-L terephthalate(2-) Chemical compound [O-]C(=O)C1=CC=C(C([O-])=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-L 0.000 description 1
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YNJBWRMUSHSURL-UHFFFAOYSA-N trichloroacetic acid Chemical compound OC(=O)C(Cl)(Cl)Cl YNJBWRMUSHSURL-UHFFFAOYSA-N 0.000 description 1
125000006000 trichloroethyl group Chemical group 0.000 description 1
229940035893 uracil Drugs 0.000 description 1
239000010455 vermiculite Substances 0.000 description 1
229910052902 vermiculite Inorganic materials 0.000 description 1
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230000037303 wrinkles Effects 0.000 description 1

Landscapes

Agricultural Chemicals And Associated Chemicals (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

DD21530878A 1978-02-14 1978-09-25 Verfahren zur herstellung von trifluormethylphenoxyphenoxycrotonsaeure-derivaten DD145748A5 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
JP1565478A JPS54109934A (en)	1978-02-14	1978-02-14	Phenoxyphenoxycrotonic acid, its preparation, and herbicides containing it

Publications (1)

Publication Number	Publication Date
DD145748A5 true DD145748A5 (de)	1981-01-07

Family

ID=11894699

Family Applications (2)

Application Number	Title	Priority Date	Filing Date
DD21530878A DD145748A5 (de)	1978-02-14	1978-09-25	Verfahren zur herstellung von trifluormethylphenoxyphenoxycrotonsaeure-derivaten
DD20807078A DD141989A5 (de)	1978-02-14	1978-09-25	Herbizides mittel

Family Applications After (1)

Application Number	Title	Priority Date	Filing Date
DD20807078A DD141989A5 (de)	1978-02-14	1978-09-25	Herbizides mittel

Country Status (7)

Country	Link
JP (1)	JPS54109934A (pl)
CA (1)	CA1082731A (pl)
DD (2)	DD145748A5 (pl)
EG (1)	EG13488A (pl)
HU (1)	HU175951B (pl)
PL (2)	PL114251B1 (pl)
SU (1)	SU1019990A3 (pl)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPS579701A (en) *	1980-06-20	1982-01-19	Kumiai Chem Ind Co Ltd	Herbicide containing optically active (+)-2-pentenoic acid compound
IN160656B (pl) *	1983-10-27	1987-07-25	Stauffer Chemical Co

1978
- 1978-02-14 JP JP1565478A patent/JPS54109934A/ja active Pending
- 1978-07-06 PL PL21626478A patent/PL114251B1/pl unknown
- 1978-07-06 PL PL20822678A patent/PL114386B1/pl unknown
- 1978-07-07 SU SU782637001A patent/SU1019990A3/ru active
- 1978-09-14 CA CA311,355A patent/CA1082731A/en not_active Expired
- 1978-09-20 HU HUKU000537 patent/HU175951B/hu unknown
- 1978-09-25 EG EG57578A patent/EG13488A/xx active
- 1978-09-25 DD DD21530878A patent/DD145748A5/de unknown
- 1978-09-25 DD DD20807078A patent/DD141989A5/de unknown

Also Published As

Publication number	Publication date
SU1019990A3 (ru)	1983-05-23
DD141989A5 (de)	1980-06-04
EG13488A (en)	1982-03-31
JPS54109934A (en)	1979-08-29
PL208226A1 (pl)	1979-10-22
PL114386B1 (en)	1981-01-31
PL114251B1 (en)	1981-01-31
HU175951B (en)	1980-11-28
CA1082731A (en)	1980-07-29

Publication	Publication Date	Title
DE2640730C2 (de)	1983-08-25	Benzoxazolyloxy- und Benzothiazolyloxy-phenoxy-Verbindungen und diese enthaltende herbizide Mittel
CH629075A5 (de)	1982-04-15	Herbizide mittel.
CH679396A5 (pl)	1992-02-14
CH640504A5 (de)	1984-01-13	Phenoxyphenoxycrotonsaeure-derivate, verfahren zur herstellung derselben, herbicide mittel mit einem gehalt derselben sowie ihre anwendung zur boden- oder blattbehandlung.
DE2611695A1 (de)	1977-09-29	Herbizide mittel
DD204607A5 (de)	1983-12-07	Herbizide und wachstumsregulierende mittel
DD201750A5 (de)	1983-08-10	Herbizide mittel
DD207847A5 (de)	1984-03-21	Herbizid
US4263040A (en)	1981-04-21	Phenoxyphenoxy unsaturated derivatives and herbicidal composition
DD145748A5 (de)	1981-01-07	Verfahren zur herstellung von trifluormethylphenoxyphenoxycrotonsaeure-derivaten
DE3009683A1 (de)	1980-09-25	N'-pyridyl-n-methylharnstoffderivate, verfahren zu ihrer herstellung und ihre verwendung als herbizide
CH641770A5 (de)	1984-03-15	Harnstoffderivate.
DE3045805A1 (de)	1982-07-08	Diphenylether, verfahren zu ihrer herstellung und ihre verwendung als herbizide
CH646941A5 (de)	1984-12-28	N-dimethylbenzylacetamidderivate.
CA1267414A (en)	1990-04-03	4h-pyrido[2,3-d][1,3]oxazin-4-one derivatives and their use for controlling undesirable plant growth
DE3123731A1 (de)	1982-12-30	Chloressigsaeurecyclohexylamide, ihre herstellung, ihre verwendung zur herbizidbekaempfung und mittel dafuer
DE3008985A1 (de)	1981-10-01	N-aryl(thiol)carbamate, verfahren zu ihrer herstellung und ihre verwendung zur bekaempfung unerwuenschten pflanzenwuchses
EP0192111B1 (de)	1990-05-16	Isoharnstoffe, Verfahren zu ihrer Herstellung und ihre Verwendung zur Bekämpfung unerwünschten Pflanzenwuchses
EP0149427B1 (de)	1987-07-08	(Poly-)Oxyalkylamino-diphenyläther mit herbizider Wirkung
EP0107123B1 (de)	1987-07-01	Anilinderivate, Verfahren zu ihrer Herstellung und ihre Verwendung zur Bekämpfung unerwünschten Pflanzenwuchses
DE3020784A1 (de)	1981-12-10	Aralkylanilinderivate und herbizide, die diese verbindungen enthalten
DE2823424A1 (de)	1979-12-13	Dibenzofuranoxylakancarbonsaeure-derivate
DD145363A5 (de)	1980-12-10	Herbizide mittel
EP0084149B1 (de)	1986-03-05	Phenoxyphenylharnstoffe, Verfahren zu ihrer Herstellung und ihre Verwendung zur Bekämpfung unerwünschten Pflanzenwuchses
DE2933917A1 (de)	1981-03-26	5-imino-imidazolidin-2-one und diese enthaltende herbizide.