RO93708B - PROCEDEU DE PREPARARE A UNOR DERIVATI DE N-(4-IZOPROPILFENIL)-2-METIL-2-PENTENAMIDA SUBSTITUITI îN POZITIA 3 A CICLULUI FENILIC, CU ACTIVITATE ERBICIDA - Google Patents
PROCEDEU DE PREPARARE A UNOR DERIVATI DE N-(4-IZOPROPILFENIL)-2-METIL-2-PENTENAMIDA SUBSTITUITI îN POZITIA 3 A CICLULUI FENILIC, CU ACTIVITATE ERBICIDAInfo
- Publication number
- RO93708B RO93708B RO121886A RO12188686A RO93708B RO 93708 B RO93708 B RO 93708B RO 121886 A RO121886 A RO 121886A RO 12188686 A RO12188686 A RO 12188686A RO 93708 B RO93708 B RO 93708B
- Authority
- RO
- Romania
- Prior art keywords
- general formula
- pentenamide
- methyl
- degrees
- group
- Prior art date
Links
- 230000002363 herbicidal effect Effects 0.000 title abstract 2
- 230000000694 effects Effects 0.000 title 1
- 239000004009 herbicide Substances 0.000 title 1
- 238000004519 manufacturing process Methods 0.000 title 1
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 abstract 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 abstract 3
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 abstract 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 abstract 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 abstract 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 abstract 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 abstract 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 abstract 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 abstract 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 abstract 2
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 abstract 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 abstract 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 abstract 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 abstract 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 abstract 2
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 abstract 2
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 abstract 2
- SSUJUUNLZQVZMO-UHFFFAOYSA-N 1,2,3,4,8,9,10,10a-octahydropyrimido[1,2-a]azepine Chemical compound C1CCC=CN2CCCNC21 SSUJUUNLZQVZMO-UHFFFAOYSA-N 0.000 abstract 1
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 abstract 1
- OCJBOOLMMGQPQU-UHFFFAOYSA-N 1,4-dichlorobenzene Chemical compound ClC1=CC=C(Cl)C=C1 OCJBOOLMMGQPQU-UHFFFAOYSA-N 0.000 abstract 1
- JJYWRQLLQAKNAD-PLNGDYQASA-N 2-methyl-2-pentenoic acid Chemical class CC\C=C(\C)C(O)=O JJYWRQLLQAKNAD-PLNGDYQASA-N 0.000 abstract 1
- SCQQBZASNXGHJU-UHFFFAOYSA-N 2-methyl-n-(4-propan-2-ylphenyl)pent-2-enamide Chemical class CCC=C(C)C(=O)NC1=CC=C(C(C)C)C=C1 SCQQBZASNXGHJU-UHFFFAOYSA-N 0.000 abstract 1
- KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 abstract 1
- JLTDJTHDQAWBAV-UHFFFAOYSA-N N,N-dimethylaniline Chemical compound CN(C)C1=CC=CC=C1 JLTDJTHDQAWBAV-UHFFFAOYSA-N 0.000 abstract 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 abstract 1
- 150000001448 anilines Chemical class 0.000 abstract 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 1
- 229910052801 chlorine Inorganic materials 0.000 abstract 1
- 239000000460 chlorine Substances 0.000 abstract 1
- 229940117389 dichlorobenzene Drugs 0.000 abstract 1
- 229910052731 fluorine Inorganic materials 0.000 abstract 1
- 125000001153 fluoro group Chemical group F* 0.000 abstract 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 150000002367 halogens Chemical group 0.000 abstract 1
- GNOIPBMMFNIUFM-UHFFFAOYSA-N hexamethylphosphoric triamide Chemical compound CN(C)P(=O)(N(C)C)N(C)C GNOIPBMMFNIUFM-UHFFFAOYSA-N 0.000 abstract 1
- 239000012442 inert solvent Substances 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- 229910052760 oxygen Inorganic materials 0.000 abstract 1
- 239000001301 oxygen Substances 0.000 abstract 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
- 229910000027 potassium carbonate Inorganic materials 0.000 abstract 1
- FVSKHRXBFJPNKK-UHFFFAOYSA-N propionitrile Chemical compound CCC#N FVSKHRXBFJPNKK-UHFFFAOYSA-N 0.000 abstract 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 abstract 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 abstract 1
- 235000017557 sodium bicarbonate Nutrition 0.000 abstract 1
- 229910000029 sodium carbonate Inorganic materials 0.000 abstract 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 abstract 1
- 239000008096 xylene Substances 0.000 abstract 1
Classifications
-
- 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
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/18—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof
- A01N37/22—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof the nitrogen atom being directly attached to an aromatic ring system, e.g. anilides
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Inventia se refera la un procedeu de preparare a unor derivati de N-(4-izopropilfenil)-2-metil-2-pentenamida substituiti în pozitia 3 a ciclului fenilic, cu activitate erbicida, cu formula generala I (vezi formula în pag.1 a descrierii) în care Y reprezinta un atom de clor sau de fluor sau o grupa metil, prin tratarea unui derivat de anilina cu formula generala II (vezi formula în pag.1 a descrierii) în care Y are semnificatiile de la formula generala I, cu un derivat de acid 2-metil-2-pentenoic cu formula generala III (vezi formula în pag.1 a descrierii) în care, atunci cînd X reprezinta halogen, n are valoarea 1 si, atunci cînd X reprezinta oxigen, n are valoarea 2, în prezenta unui solvent inert ales din grupa constituita din benzen, toluen, xilen, clorbenzen, diclorbenzen, acetona, metiletilcetona, acetonitril, propionitril, eter etilic, tetrahidrofuran, dioxan, dimetilformamida, dimetilsulfoxid si hexametilfosforamida, si a unui acceptor de acid ales din grupa constituita din trietilamina, piridina, dimetilanilina, 1,8-diazabiciclo-(5,4,0)-undecen, carbonat de potasiu, carbonat de sodiu, hidroxid de sodiu, hidroxid de potasiu si bicarbonat de sodiu, la o temperatura cuprinsa între -10 si 150 degree C, de preferinta între 5 si 90 degree C si, în special, între 15 si 70 degree C.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP414485A JPS61165356A (ja) | 1985-01-16 | 1985-01-16 | Ｎ−（３−メチル−４−イソプロピルフエニル）カルボン酸アミド誘導体および選択性殺草剤 |
| JP876485A JPS61167653A (ja) | 1985-01-21 | 1985-01-21 | Ｎ−（３−ハロゲノ−４−イソプロピルフエニル）−２−メチル−２−ペンテン酸アミド誘導体および選択性殺草剤 |
| JP876385A JPH066561B2 (ja) | 1985-01-21 | 1985-01-21 | Ｎ−（３−クロロ−４−イソプロピルフエニル）−２−メチル−２−ペンテン酸アミドおよび選択性殺草剤 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| RO93708A RO93708A (ro) | 1988-03-30 |
| RO93708B true RO93708B (ro) | 1988-03-31 |
Family
ID=27276135
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| RO121886A RO93708B (ro) | 1985-01-16 | 1986-01-16 | PROCEDEU DE PREPARARE A UNOR DERIVATI DE N-(4-IZOPROPILFENIL)-2-METIL-2-PENTENAMIDA SUBSTITUITI îN POZITIA 3 A CICLULUI FENILIC, CU ACTIVITATE ERBICIDA |
Country Status (7)
| Country | Link |
|---|---|
| AU (1) | AU5212786A (ro) |
| DE (1) | DE3601148A1 (ro) |
| FR (1) | FR2576016B1 (ro) |
| GB (1) | GB2170500B (ro) |
| HU (1) | HUT41208A (ro) |
| IT (1) | IT1191847B (ro) |
| RO (1) | RO93708B (ro) |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL238969A (ro) * | 1958-05-06 | |||
| JPS6023357A (ja) * | 1983-07-19 | 1985-02-05 | Mitsui Toatsu Chem Inc | ２−メチル−４′−イソプロピル−２−ペンテノイルアニリドおよび選択性殺草剤 |
-
1986
- 1986-01-09 AU AU52127/86A patent/AU5212786A/en not_active Abandoned
- 1986-01-14 GB GB08600788A patent/GB2170500B/en not_active Expired
- 1986-01-15 HU HU86210A patent/HUT41208A/hu unknown
- 1986-01-16 DE DE19863601148 patent/DE3601148A1/de not_active Withdrawn
- 1986-01-16 FR FR8600567A patent/FR2576016B1/fr not_active Expired
- 1986-01-16 IT IT19095/86A patent/IT1191847B/it active
- 1986-01-16 RO RO121886A patent/RO93708B/ro unknown
Also Published As
| Publication number | Publication date |
|---|---|
| IT8619095A0 (it) | 1986-01-16 |
| IT1191847B (it) | 1988-03-23 |
| DE3601148A1 (de) | 1986-07-17 |
| GB2170500B (en) | 1988-07-27 |
| FR2576016B1 (fr) | 1987-11-20 |
| AU5212786A (en) | 1986-07-24 |
| FR2576016A1 (fr) | 1986-07-18 |
| GB2170500A (en) | 1986-08-06 |
| HUT41208A (en) | 1987-04-28 |
| GB8600788D0 (en) | 1986-02-19 |
| RO93708A (ro) | 1988-03-30 |
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