SU1230466A3 - Способ получени алкилтиокарбаматов - Google Patents

Способ получени алкилтиокарбаматов Download PDF

Info

Publication number: SU1230466A3
Authority: SU; USSR - Soviet Union
Prior art keywords: amine; lower alkyl; producing; alkylthiocarbamates; general formula
Prior art date: 1976-10-04

Application number

SU772528002A

Other languages

English (en)

Russian (ru)

Inventor

Махонрэй Питт Гарольд

Original Assignee

Стауффер Кемикал Компани (Фирма)

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.)

1976-10-04

Filing date

1977-10-04

Publication date

1986-05-07

1977-10-04 Application filed by Стауффер Кемикал Компани (Фирма) filed Critical Стауффер Кемикал Компани (Фирма)

1986-05-07 Application granted granted Critical

1986-05-07 Publication of SU1230466A3 publication Critical patent/SU1230466A3/ru

Links

238000000034 method Methods 0.000 title description 4
JJWKPURADFRFRB-UHFFFAOYSA-N carbonyl sulfide Chemical compound O=C=S JJWKPURADFRFRB-UHFFFAOYSA-N 0.000 claims description 8
125000000217 alkyl group Chemical group 0.000 claims description 6
150000001412 amines Chemical class 0.000 claims description 5
238000004519 manufacturing process Methods 0.000 claims description 3
125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 2
150000001348 alkyl chlorides Chemical class 0.000 claims 2
230000003993 interaction Effects 0.000 claims 1
239000000203 mixture Substances 0.000 claims 1
241000196324 Embryophyta Species 0.000 description 8
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 6
150000001875 compounds Chemical class 0.000 description 6
230000006378 damage Effects 0.000 description 6
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 5
230000002363 herbicidal effect Effects 0.000 description 5
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
239000007788 liquid Substances 0.000 description 4
239000002689 soil Substances 0.000 description 4
235000007319 Avena orientalis Nutrition 0.000 description 3
244000075850 Avena orientalis Species 0.000 description 3
241000219198 Brassica Species 0.000 description 3
235000003351 Brassica cretica Nutrition 0.000 description 3
235000003343 Brassica rupestris Nutrition 0.000 description 3
244000058871 Echinochloa crus-galli Species 0.000 description 3
244000046052 Phaseolus vulgaris Species 0.000 description 3
235000010627 Phaseolus vulgaris Nutrition 0.000 description 3
238000002474 experimental method Methods 0.000 description 3
235000010460 mustard Nutrition 0.000 description 3
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
239000002904 solvent Substances 0.000 description 3
239000007921 spray Substances 0.000 description 3
240000001592 Amaranthus caudatus Species 0.000 description 2
235000009328 Amaranthus caudatus Nutrition 0.000 description 2
240000004153 Hibiscus sabdariffa Species 0.000 description 2
235000001018 Hibiscus sabdariffa Nutrition 0.000 description 2
235000015225 Panicum colonum Nutrition 0.000 description 2
229920001213 Polysorbate 20 Polymers 0.000 description 2
235000005291 Rumex acetosa Nutrition 0.000 description 2
235000012735 amaranth Nutrition 0.000 description 2
239000004178 amaranth Substances 0.000 description 2
QKSKPIVNLNLAAV-UHFFFAOYSA-N bis(2-chloroethyl) sulfide Chemical compound ClCCSCCCl QKSKPIVNLNLAAV-UHFFFAOYSA-N 0.000 description 2
-1 butyl butyl Chemical group 0.000 description 2
239000007795 chemical reaction product Substances 0.000 description 2
HRYZWHHZPQKTII-UHFFFAOYSA-N chloroethane Chemical compound CCCl HRYZWHHZPQKTII-UHFFFAOYSA-N 0.000 description 2
229960003750 ethyl chloride Drugs 0.000 description 2
238000003306 harvesting Methods 0.000 description 2
239000000256 polyoxyethylene sorbitan monolaurate Substances 0.000 description 2
235000010486 polyoxyethylene sorbitan monolaurate Nutrition 0.000 description 2
239000000047 product Substances 0.000 description 2
235000003513 sheep sorrel Nutrition 0.000 description 2
PLFFHJWXOGYWPR-HEDMGYOXSA-N (4r)-4-[(3r,3as,5ar,5br,7as,11as,11br,13ar,13bs)-5a,5b,8,8,11a,13b-hexamethyl-1,2,3,3a,4,5,6,7,7a,9,10,11,11b,12,13,13a-hexadecahydrocyclopenta[a]chrysen-3-yl]pentan-1-ol Chemical compound C([C@]1(C)[C@H]2CC[C@H]34)CCC(C)(C)[C@@H]1CC[C@@]2(C)[C@]4(C)CC[C@@H]1[C@]3(C)CC[C@@H]1[C@@H](CCCO)C PLFFHJWXOGYWPR-HEDMGYOXSA-N 0.000 description 1
NJBCRXCAPCODGX-UHFFFAOYSA-N 2-methyl-n-(2-methylpropyl)propan-1-amine Chemical compound CC(C)CNCC(C)C NJBCRXCAPCODGX-UHFFFAOYSA-N 0.000 description 1
241001390821 Boerhavia repens Species 0.000 description 1
235000011332 Brassica juncea Nutrition 0.000 description 1
244000178993 Brassica juncea Species 0.000 description 1
235000014700 Brassica juncea var napiformis Nutrition 0.000 description 1
244000025254 Cannabis sativa Species 0.000 description 1
244000152970 Digitaria sanguinalis Species 0.000 description 1
235000010823 Digitaria sanguinalis Nutrition 0.000 description 1
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
240000005561 Musa balbisiana Species 0.000 description 1
235000018290 Musa x paradisiaca Nutrition 0.000 description 1
235000011999 Panicum crusgalli Nutrition 0.000 description 1
244000115721 Pennisetum typhoides Species 0.000 description 1
235000007195 Pennisetum typhoides Nutrition 0.000 description 1
229920001214 Polysorbate 60 Polymers 0.000 description 1
240000004284 Rumex crispus Species 0.000 description 1
235000021501 Rumex crispus Nutrition 0.000 description 1
235000008515 Setaria glauca Nutrition 0.000 description 1
239000008346 aqueous phase Substances 0.000 description 1
206010012601 diabetes mellitus Diseases 0.000 description 1
239000003995 emulsifying agent Substances 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
230000003203 everyday effect Effects 0.000 description 1
230000035784 germination Effects 0.000 description 1
239000004009 herbicide Substances 0.000 description 1
DKAGJZJALZXOOV-UHFFFAOYSA-N hydrate;hydrochloride Chemical compound O.Cl DKAGJZJALZXOOV-UHFFFAOYSA-N 0.000 description 1
239000006199 nebulizer Substances 0.000 description 1
239000012074 organic phase Substances 0.000 description 1
235000005919 possum grape Nutrition 0.000 description 1
238000009331 sowing Methods 0.000 description 1
241000894007 species Species 0.000 description 1
239000000126 substance Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/16—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms
- C07D295/20—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms by radicals derived from carbonic acid, or sulfur or nitrogen analogues thereof
- C07D295/21—Radicals derived from sulfur analogues of carbonic acid
- 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
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/10—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof

Landscapes

Life Sciences & Earth Sciences (AREA)
Organic Chemistry (AREA)
Chemical & Material Sciences (AREA)
Dentistry (AREA)
Health & Medical Sciences (AREA)
Engineering & Computer Science (AREA)
Plant Pathology (AREA)
General Health & Medical Sciences (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Environmental Sciences (AREA)
Pest Control & Pesticides (AREA)
Agronomy & Crop Science (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)

SU772528002A 1976-10-04 1977-10-04 Способ получени алкилтиокарбаматов SU1230466A3 (ru)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US72956976A	1976-10-04	1976-10-04

Publications (1)

Publication Number	Publication Date
SU1230466A3 true SU1230466A3 (ru)	1986-05-07

Family

ID=24931635

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
SU772528002A SU1230466A3 (ru)	1976-10-04	1977-10-04	Способ получени алкилтиокарбаматов

Country Status (5)

Country	Link
BE (1)	BE859097A (cs)
CS (1)	CS196390B2 (cs)
HU (1)	HU175661B (cs)
SU (1)	SU1230466A3 (cs)
ZA (1)	ZA775874B (cs)

1977
- 1977-09-28 BE BE2056284A patent/BE859097A/nl not_active IP Right Cessation
- 1977-09-30 HU HU77SA3062A patent/HU175661B/hu not_active IP Right Cessation
- 1977-10-03 CS CS776366A patent/CS196390B2/cs unknown
- 1977-10-03 ZA ZA00775874A patent/ZA775874B/xx unknown
- 1977-10-04 SU SU772528002A patent/SU1230466A3/ru active

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
Патент US № 3836524, кл. С 07 С 155/02, опублик. 1975. Патент US № 3954729, кл. С 07 С 155/02, опублик. 1976. *

Also Published As

Publication number	Publication date
CS196390B2 (cs)	1980-03-31
ZA775874B (en)	1978-05-30
BE859097A (nl)	1978-03-28
HU175661B (hu)	1980-09-28

Publication	Publication Date	Title
DE2515091C2 (de)	1987-04-16	N-Acyl-N-phenyl-alaninderivate und -glycinderivate, Verfahren zu deren Herstellung und diese Verbindungen enthaltende fungizide Mittel
EP3057427B1 (en)	2018-07-18	Processes for the preparation of pesticidal compounds
DE4011172A1 (de)	1991-10-10	Verbindungen zur bekaempfung von pflanzenkrankheiten
US3976470A (en)	1976-08-24	Diphenyl ether amides
SU1169516A3 (ru)	1985-07-23	Способ борьбы с нежелательной растительностью
US3168561A (en)	1965-02-02	N-alkoxy 2-alkyl-4-chlorophenoxyacetamides for the control of pests
SU1068036A3 (ru)	1984-01-15	Способ получени кристаллической смеси @ -цис- @ -и @ цис- @ -изомеров производных циклопропанкарбоновых кислот в эквимол рном соотношении
SU1230466A3 (ru)	1986-05-07	Способ получени алкилтиокарбаматов
SU1412595A3 (ru)	1988-07-23	Способ борьбы с нежелательной растительностью
US3166591A (en)	1965-01-19	Phenoxyacetamides for the control of pests
SU955862A3 (ru)	1982-08-30	Способ получени аминовых солей замещенных N-фосфонометилмочевин
US3872157A (en)	1975-03-18	Substituted anilide carbamates
CH616687A5 (cs)	1980-04-15
DE2112643C3 (de)	1981-02-19	Formamidin-Derivate und sie enthaltende Mittel
US3493360A (en)	1970-02-03	Herbicides
US3971649A (en)	1976-07-27	S-methyl-N-[4-(4'-chlorophenoxy)phenyl] thiolcarbamate
DE2451512A1 (de)	1975-05-15	Substituierte succinamide, verfahren zu ihrer herstellung und ihre verwendung als herbizide
CS214799B2 (cs)	1982-05-28	Prostředek k regulaci růstu rostlin a způsob výroby účinných látek
US2916369A (en)	1959-12-08	Diallylthiolcarbamates and their use as herbicides
US4066440A (en)	1978-01-03	Symmetrical alkynyl ureas
CA1080240A (en)	1980-06-24	Preparation of esters of thiocarbamic acids
DE2745229C2 (de)	1986-03-27	4-Alkylsulfonyloxyphenyl-N-alkylthiocarbamate, Verfahren zu ihrer Herstellung und ihre Verwendung als Fungizide
CH626229A5 (cs)	1981-11-13
US3628945A (en)	1971-12-21	Selectively herbicidal 3-substituted-2-halopropyl thiolcarbamates and method of combating undesired vegetation
US3352897A (en)	1967-11-14	Nu-alkoxy amides of 4-halophenoxyalkylcarboxy acids