ES341454A1 - Procedimiento para preparar anilinoalcohil carboxamidas. - Google Patents

Procedimiento para preparar anilinoalcohil carboxamidas.

Info

Publication number: ES341454A1
Authority: ES; Spain
Prior art keywords: group; atom; alkyl; substituted; hydrogen
Prior art date: 1966-06-08
Legal status (The legal status 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 status listed.): Expired

Application number

ES341454A

Other languages

English (en)

Spanish (es)

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

SHELL INT RESEARCH

Shell Internationale Research Maatschappij BV

Original Assignee

SHELL INT RESEARCH

Shell Internationale Research Maatschappij BV

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.)

1966-06-08

Filing date

1967-06-06

Publication date

1968-12-01

1967-06-06 Application filed by SHELL INT RESEARCH, Shell Internationale Research Maatschappij BV filed Critical SHELL INT RESEARCH

1968-12-01 Publication of ES341454A1 publication Critical patent/ES341454A1/es

Status Expired legal-status Critical Current

Links

230000002363 herbicidal effect Effects 0.000 title abstract 2
239000000203 mixture Substances 0.000 title abstract 2
150000001875 compounds Chemical class 0.000 abstract 8
125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 8
125000000217 alkyl group Chemical group 0.000 abstract 7
125000004432 carbon atom Chemical group C* 0.000 abstract 5
125000003118 aryl group Chemical group 0.000 abstract 4
125000006575 electron-withdrawing group Chemical group 0.000 abstract 4
FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 abstract 4
NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 abstract 3
239000004094 surface-active agent Substances 0.000 abstract 3
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 abstract 2
KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 abstract 2
PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 abstract 2
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 2
BAVYZALUXZFZLV-UHFFFAOYSA-N Methylamine Chemical compound NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 abstract 2
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 abstract 2
239000002253 acid Substances 0.000 abstract 2
239000004480 active ingredient Substances 0.000 abstract 2
125000003342 alkenyl group Chemical group 0.000 abstract 2
125000004390 alkyl sulfonyl group Chemical group 0.000 abstract 2
125000002947 alkylene group Chemical group 0.000 abstract 2
150000001412 amines Chemical class 0.000 abstract 2
125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 abstract 2
229910052801 chlorine Inorganic materials 0.000 abstract 2
239000000460 chlorine Substances 0.000 abstract 2
125000004093 cyano group Chemical group *C#N 0.000 abstract 2
150000002148 esters Chemical class 0.000 abstract 2
229910052731 fluorine Inorganic materials 0.000 abstract 2
239000011737 fluorine Substances 0.000 abstract 2
125000005843 halogen group Chemical group 0.000 abstract 2
125000005842 heteroatom Chemical group 0.000 abstract 2
125000000623 heterocyclic group Chemical group 0.000 abstract 2
229910052739 hydrogen Inorganic materials 0.000 abstract 2
239000001257 hydrogen Substances 0.000 abstract 2
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 2
229910052757 nitrogen Inorganic materials 0.000 abstract 2
125000004433 nitrogen atom Chemical group 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
125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 2
KLNIWDWRMUMRQA-UHFFFAOYSA-N 2-(2,6-dinitroanilino)propanoic acid Chemical compound OC(=O)C(C)NC1=C([N+]([O-])=O)C=CC=C1[N+]([O-])=O KLNIWDWRMUMRQA-UHFFFAOYSA-N 0.000 abstract 1
BPPMIQPXQVIZNJ-UHFFFAOYSA-N 2-chloro-1,3-dinitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC([N+]([O-])=O)=C1Cl BPPMIQPXQVIZNJ-UHFFFAOYSA-N 0.000 abstract 1
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 abstract 1
QNAYBMKLOCPYGJ-REOHCLBHSA-N L-alanine Chemical compound C[C@H](N)C(O)=O QNAYBMKLOCPYGJ-REOHCLBHSA-N 0.000 abstract 1
150000001413 amino acids Chemical class 0.000 abstract 1
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 1
239000000969 carrier Substances 0.000 abstract 1
-1 dusts Substances 0.000 abstract 1
239000004495 emulsifiable concentrate Substances 0.000 abstract 1
239000000839 emulsion Substances 0.000 abstract 1
239000008187 granular material Substances 0.000 abstract 1
XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 abstract 1
239000012442 inert solvent Substances 0.000 abstract 1
239000006072 paste Substances 0.000 abstract 1
229910000027 potassium carbonate Inorganic materials 0.000 abstract 1
239000000843 powder Substances 0.000 abstract 1
QLNJFJADRCOGBJ-UHFFFAOYSA-N propionamide Chemical compound CCC(N)=O QLNJFJADRCOGBJ-UHFFFAOYSA-N 0.000 abstract 1
229940080818 propionamide Drugs 0.000 abstract 1
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 abstract 1
CDBYLPFSWZWCQE-UHFFFAOYSA-L sodium carbonate Substances [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 abstract 1
229910000029 sodium carbonate Inorganic materials 0.000 abstract 1
239000000243 solution Substances 0.000 abstract 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C255/00—Carboxylic acid nitriles
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C243/00—Compounds containing chains of nitrogen atoms singly-bound to each other, e.g. hydrazines, triazanes
- C07C243/24—Hydrazines having nitrogen atoms of hydrazine groups acylated by carboxylic acids
- C07C243/26—Hydrazines having nitrogen atoms of hydrazine groups acylated by carboxylic acids with acylating carboxyl groups bound to hydrogen atoms or to acyclic carbon atoms
- C07C243/34—Hydrazines having nitrogen atoms of hydrazine groups acylated by carboxylic acids with acylating carboxyl groups bound to hydrogen atoms or to acyclic carbon atoms to carbon atoms of a carbon skeleton further substituted by nitrogen atoms

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)

ES341454A 1966-06-08 1967-06-06 Procedimiento para preparar anilinoalcohil carboxamidas. Expired ES341454A1 (es)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
GB25473/66A GB1122043A (en)	1966-06-08	1966-06-08	Anilinoalkylcarboxamides and herbicidal compositions containing them

Publications (1)

Publication Number	Publication Date
ES341454A1 true ES341454A1 (es)	1968-12-01

Family

ID=10228289

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
ES341454A Expired ES341454A1 (es)	1966-06-08	1967-06-06	Procedimiento para preparar anilinoalcohil carboxamidas.

Country Status (9)

Country	Link
BE (1)	BE699557A (de)
CH (1)	CH501358A (de)
DE (1)	DE1642337C3 (de)
DK (1)	DK118797B (de)
ES (1)	ES341454A1 (de)
GB (1)	GB1122043A (de)
NL (1)	NL159088B (de)
OA (1)	OA02447A (de)
SE (1)	SE359090B (de)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4243819A (en) *	1978-02-16	1981-01-06	Zoecon Corporation	Substituted amino acids
EP0025616B1 (de) *	1979-08-28	1983-11-30	Shell Internationale Researchmaatschappij B.V.	Ein Verfahren zur Lockerung von Früchten und/oder Blättern
CA3143132A1 (en) *	2019-06-11	2020-12-17	Fortephest Ltd.	Novel non-coding heterocyclic amino acids (nchaa) and their use as herbicides

1966
- 1966-06-08 GB GB25473/66A patent/GB1122043A/en not_active Expired
1967
- 1967-06-05 OA OA52963A patent/OA02447A/xx unknown
- 1967-06-06 BE BE699557D patent/BE699557A/xx unknown
- 1967-06-06 ES ES341454A patent/ES341454A1/es not_active Expired
- 1967-06-06 CH CH795867A patent/CH501358A/de not_active IP Right Cessation
- 1967-06-06 DK DK296367AA patent/DK118797B/da unknown
- 1967-06-06 DE DE1642337A patent/DE1642337C3/de not_active Expired
- 1967-06-06 SE SE07887/67A patent/SE359090B/xx unknown
- 1967-06-07 NL NL6707890.A patent/NL159088B/xx not_active IP Right Cessation

Also Published As

Publication number	Publication date
OA02447A (fr)	1970-05-05
DE1642337A1 (de)	1971-07-29
BE699557A (de)	1967-12-06
DE1642337C3 (de)	1979-09-27
SE359090B (de)	1973-08-20
DK118797B (da)	1970-10-05
NL6707890A (de)	1967-12-11
CH501358A (de)	1971-01-15
GB1122043A (en)	1968-07-31
DE1642337B2 (de)	1979-01-18
NL159088B (nl)	1979-01-15

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