MD419C2 - Process for stereoselective allyl chlorides Z-1,2-diaryl preparation - Google Patents
Process for stereoselective allyl chlorides Z-1,2-diaryl preparationInfo
- Publication number
- MD419C2 MD419C2 MD95-0220A MD950220A MD419C2 MD 419 C2 MD419 C2 MD 419C2 MD 950220 A MD950220 A MD 950220A MD 419 C2 MD419 C2 MD 419C2
- Authority
- MD
- Moldova
- Prior art keywords
- preparation
- halogen
- stereoselective
- diaryl
- ether
- Prior art date
Links
- 238000000034 method Methods 0.000 title abstract 3
- 230000000707 stereoselective effect Effects 0.000 title abstract 2
- -1 allyl chlorides Chemical class 0.000 title 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 abstract 4
- OSDWBNJEKMUWAV-UHFFFAOYSA-N Allyl chloride Chemical compound ClCC=C OSDWBNJEKMUWAV-UHFFFAOYSA-N 0.000 abstract 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- 125000003545 alkoxy group Chemical group 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 230000000843 anti-fungal effect Effects 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- 150000001244 carboxylic acid anhydrides Chemical class 0.000 abstract 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 abstract 1
- 230000000855 fungicidal effect Effects 0.000 abstract 1
- 239000000417 fungicide Substances 0.000 abstract 1
- 125000004438 haloalkoxy group Chemical group 0.000 abstract 1
- 125000001188 haloalkyl group Chemical group 0.000 abstract 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 150000002367 halogens Chemical class 0.000 abstract 1
- 239000013067 intermediate product Substances 0.000 abstract 1
- 150000002576 ketones Chemical class 0.000 abstract 1
- 239000000463 material Substances 0.000 abstract 1
- 235000015097 nutrients Nutrition 0.000 abstract 1
- 230000000144 pharmacologic effect Effects 0.000 abstract 1
- 239000002904 solvent Substances 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C17/00—Preparation of halogenated hydrocarbons
- C07C17/35—Preparation of halogenated hydrocarbons by reactions not affecting the number of carbon or of halogen atoms in the reaction
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C25/00—Compounds containing at least one halogen atom bound to a six-membered aromatic ring
- C07C25/24—Halogenated aromatic hydrocarbons with unsaturated side chains
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C43/00—Ethers; Compounds having groups, groups or groups
- C07C43/02—Ethers
- C07C43/20—Ethers having an ether-oxygen atom bound to a carbon atom of a six-membered aromatic ring
- C07C43/225—Ethers having an ether-oxygen atom bound to a carbon atom of a six-membered aromatic ring containing halogen
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C43/00—Ethers; Compounds having groups, groups or groups
- C07C43/02—Ethers
- C07C43/257—Ethers having an ether-oxygen atom bound to carbon atoms both belonging to six-membered aromatic rings
- C07C43/29—Ethers having an ether-oxygen atom bound to carbon atoms both belonging to six-membered aromatic rings containing halogen
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/12—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/56—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D303/00—Compounds containing three-membered rings having one oxygen atom as the only ring hetero atom
- C07D303/02—Compounds containing oxirane rings
- C07D303/08—Compounds containing oxirane rings with hydrocarbon radicals, substituted by halogen atoms, nitro radicals or nitroso radicals
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Epoxy Compounds (AREA)
Abstract
The problem of the present invention consists in the process elaboration corresponding to which it is possible to obtain allyl chloride Z-1,2-diaryl high yield of the general formulaused as intermediate products at preparation of the pharmacologic, fungicide and anti-fungal primary nutrient basis.The process for stereoselective materials preparation of the general formula (I) consists in the fact, that the chlorhydrines of formula (II)where the rests R1 and R2 independently from each other represent hydrogene, halogen, alkyl, halogen alkyl, alkoxy, halogen alkoxy or unsubstituted or substituted aromatic rest, and n and m represent 1,2 or 3 are dehydrated in the inerte ether or ether of carboxylic acid as solvent in presence of carboxylic acid anhydride or corresponding ketone and organic or unorganic acid or oleum at the temperature up to 50°C.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE3923674A DE3923674A1 (en) | 1989-07-18 | 1989-07-18 | New 1,2-di:aryl-3-chloro-propene cpds. |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MD419C2 true MD419C2 (en) | 1996-07-31 |
Family
ID=6385245
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MD95-0220A MD419C2 (en) | 1989-07-18 | 1994-12-13 | Process for stereoselective allyl chlorides Z-1,2-diaryl preparation |
Country Status (4)
| Country | Link |
|---|---|
| DE (1) | DE3923674A1 (en) |
| MD (1) | MD419C2 (en) |
| RU (2) | RU2014317C1 (en) |
| UA (1) | UA37175C2 (en) |
-
1989
- 1989-07-18 DE DE3923674A patent/DE3923674A1/en not_active Withdrawn
-
1990
- 1990-07-17 UA UA4830460A patent/UA37175C2/en unknown
- 1990-07-17 RU SU904830460A patent/RU2014317C1/en active
-
1991
- 1991-11-26 RU RU94011635A patent/RU2125997C1/en not_active IP Right Cessation
-
1994
- 1994-12-13 MD MD95-0220A patent/MD419C2/en not_active IP Right Cessation
Non-Patent Citations (4)
| Title |
|---|
| Brevet nr. 3218129, DE, Int. Cl. C 07 D 405/06, 1983. * |
| Brevet nr. 3218130, DE, Int. Cl. C 07 D 405/06, 1983. * |
| Brevet, nr. 196038, Ep, Int. Cl. C 07 D 405/06, 1983. * |
| Houben-Weyl. Meth. der organ. Chemie, ediţia 4, vol. 5/1, 1972, p. 62-71. * |
Also Published As
| Publication number | Publication date |
|---|---|
| RU2014317C1 (en) | 1994-06-15 |
| DE3923674A1 (en) | 1991-01-31 |
| UA37175C2 (en) | 2001-05-15 |
| RU2125997C1 (en) | 1999-02-10 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DK469589A (en) | 7-SUBSTITUTED DERIVATIVES OF 3,5-DIHYDROXYHEPT-6-ACID ACID, THEIR PREPARATION AND USE, AND THE PRODUCTION USED INTERMEDIATES | |
| RO104615B1 (en) | Preparation method of 7-fluor-1-methyl-3-methylsulphonyl -4-quinoline | |
| DE69122866D1 (en) | PRODUCTION OF SUBSTITUTED PIPERIDINES | |
| DE2961012D1 (en) | Fluor-containing 1,4-dihydropyridines, pharmaceuticals containing them and process for their preparation | |
| ATE192743T1 (en) | METHOD FOR PRODUCING 2-(2',4'-DIHYDROXYPHENYL)-4,6-DIARYL-S-TRIAZINE | |
| MD419C2 (en) | Process for stereoselective allyl chlorides Z-1,2-diaryl preparation | |
| ES2143459T3 (en) | 4,5-DIHIDRO-1H-PIRAZOL-1-CARBOXAMIDAS N-ARIL-3-ARIL-4 SUBSTITUTED AND PROCEDURES FOR ITS PRODUCTION. | |
| HU904344D0 (en) | Process for stereoselective production of 2-1,2-diaryl-allylchlorides as well as for transformation of these compounds into azolyl-methyl-oxyranes | |
| KR870005954A (en) | Improved process for preparing 5- (2,5-dimethylphenoxy) -2,2-dimethylpentanoic acid | |
| EP0187674A2 (en) | Process for the preparation of polyhalogenated carbinols | |
| FR2377382A1 (en) | NEW PHENYLAZACYCLOALCANES USEFUL AS MEDICINAL PRODUCTS | |
| EP0230948A3 (en) | Benzoylacetic acid ester derivatives and process for their preparation | |
| GB1189514A (en) | New Cyclic Ketones | |
| JPS577438A (en) | Production of acid chloride | |
| US5360919A (en) | Polycyclic dyes | |
| JPS5540653A (en) | Perhydropyrroloimidazole derivative, and agricultural and horticultural fungicide comprising it | |
| DK0801897T3 (en) | Composition and process for the preparation of the composition, as well as raw materials, products and means of production | |
| US3125582A (en) | Phenylvinylene cyclic carbonates | |
| JPS55108828A (en) | Preparation of chlorination product and ethyl benzene | |
| SU404824A1 (en) | PTB | |
| ES2045098T3 (en) | PROCEDURE FOR THE PREPARATION OF THIAZOLOBENCIMIDAZOLES AND INTERMEDIATE PRODUCTS USED IN THE. | |
| DE3575419D1 (en) | METHOD FOR THE PRODUCTION OF ALPHA HYDROXYAL CALCAR CARBON ACIDS. | |
| KR970707134A (en) | Process for the Preparation of 1-Halo-3-Trialkylsilanyl-Benzene Derivatives | |
| JPS5659727A (en) | Preparation of substituted phenol | |
| KR890701511A (en) | Dehydrobromination of Substituted α-halocumen |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| KA4A | Patent for invention lapsed due to non-payment of fees (with right of restoration) | ||
| MM4A | Patent for invention definitely lapsed due to non-payment of fees |