NL7905556A - Nieuw tussenprodukt bij de bereiding van esters van cyclopropaancarbonzuren en werkwijze ter bereiding van het tussenprodukt. - Google Patents
Nieuw tussenprodukt bij de bereiding van esters van cyclopropaancarbonzuren en werkwijze ter bereiding van het tussenprodukt. Download PDFInfo
- Publication number
- NL7905556A NL7905556A NL7905556A NL7905556A NL7905556A NL 7905556 A NL7905556 A NL 7905556A NL 7905556 A NL7905556 A NL 7905556A NL 7905556 A NL7905556 A NL 7905556A NL 7905556 A NL7905556 A NL 7905556A
- Authority
- NL
- Netherlands
- Prior art keywords
- preparation
- esters
- formula
- preparing
- compound
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims description 11
- 238000004519 manufacturing process Methods 0.000 title claims description 3
- 238000002360 preparation method Methods 0.000 title description 10
- 239000013067 intermediate product Substances 0.000 title description 3
- 150000004653 carbonic acids Chemical class 0.000 title 1
- -1 Cyclopropane compound Chemical class 0.000 claims description 8
- 150000001875 compounds Chemical class 0.000 claims description 8
- BQOFWKZOCNGFEC-BDAKNGLRSA-N (+)-Delta3-carene Chemical compound C1C(C)=CC[C@H]2C(C)(C)[C@@H]12 BQOFWKZOCNGFEC-BDAKNGLRSA-N 0.000 claims description 7
- 229930006713 (+)-car-3-ene Natural products 0.000 claims description 7
- BQOFWKZOCNGFEC-UHFFFAOYSA-N Delta3-Carene Natural products C1C(C)=CCC2C(C)(C)C12 BQOFWKZOCNGFEC-UHFFFAOYSA-N 0.000 claims description 7
- 239000007858 starting material Substances 0.000 claims description 4
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims description 3
- BSDTVZZPJYPNDF-UHFFFAOYSA-N [1-(2,2-dimethoxyethyl)-2,2-dimethylcyclopropyl]methyl acetate Chemical compound COC(OC)CC1(COC(C)=O)CC1(C)C BSDTVZZPJYPNDF-UHFFFAOYSA-N 0.000 claims description 2
- 229950011148 cyclopropane Drugs 0.000 claims 2
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
- 150000002148 esters Chemical class 0.000 description 8
- 239000000543 intermediate Substances 0.000 description 5
- NLFBCYMMUAKCPC-KQQUZDAGSA-N ethyl (e)-3-[3-amino-2-cyano-1-[(e)-3-ethoxy-3-oxoprop-1-enyl]sulfanyl-3-oxoprop-1-enyl]sulfanylprop-2-enoate Chemical compound CCOC(=O)\C=C\SC(=C(C#N)C(N)=O)S\C=C\C(=O)OCC NLFBCYMMUAKCPC-KQQUZDAGSA-N 0.000 description 4
- 230000000749 insecticidal effect Effects 0.000 description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- YMGUBTXCNDTFJI-UHFFFAOYSA-N cyclopropanecarboxylic acid Chemical class OC(=O)C1CC1 YMGUBTXCNDTFJI-UHFFFAOYSA-N 0.000 description 3
- 239000002917 insecticide Substances 0.000 description 3
- 239000002728 pyrethroid Substances 0.000 description 3
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- 230000002378 acidificating effect Effects 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 2
- 230000007062 hydrolysis Effects 0.000 description 2
- 238000006460 hydrolysis reaction Methods 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 230000000707 stereoselective effect Effects 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 150000003505 terpenes Chemical class 0.000 description 2
- 235000007586 terpenes Nutrition 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- AOSZTAHDEDLTLQ-AZKQZHLXSA-N (1S,2S,4R,8S,9S,11S,12R,13S,19S)-6-[(3-chlorophenyl)methyl]-12,19-difluoro-11-hydroxy-8-(2-hydroxyacetyl)-9,13-dimethyl-6-azapentacyclo[10.8.0.02,9.04,8.013,18]icosa-14,17-dien-16-one Chemical compound C([C@@H]1C[C@H]2[C@H]3[C@]([C@]4(C=CC(=O)C=C4[C@@H](F)C3)C)(F)[C@@H](O)C[C@@]2([C@@]1(C1)C(=O)CO)C)N1CC1=CC=CC(Cl)=C1 AOSZTAHDEDLTLQ-AZKQZHLXSA-N 0.000 description 1
- GVNVAWHJIKLAGL-UHFFFAOYSA-N 2-(cyclohexen-1-yl)cyclohexan-1-one Chemical compound O=C1CCCCC1C1=CCCCC1 GVNVAWHJIKLAGL-UHFFFAOYSA-N 0.000 description 1
- YNJSNEKCXVFDKW-UHFFFAOYSA-N 3-(5-amino-1h-indol-3-yl)-2-azaniumylpropanoate Chemical compound C1=C(N)C=C2C(CC(N)C(O)=O)=CNC2=C1 YNJSNEKCXVFDKW-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- 240000007124 Brassica oleracea Species 0.000 description 1
- 235000003899 Brassica oleracea var acephala Nutrition 0.000 description 1
- 235000011301 Brassica oleracea var capitata Nutrition 0.000 description 1
- 235000001169 Brassica oleracea var oleracea Nutrition 0.000 description 1
- 101150065749 Churc1 gene Proteins 0.000 description 1
- 229940126657 Compound 17 Drugs 0.000 description 1
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 1
- 238000005481 NMR spectroscopy Methods 0.000 description 1
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 1
- 102100038239 Protein Churchill Human genes 0.000 description 1
- HEDRZPFGACZZDS-MICDWDOJSA-N Trichloro(2H)methane Chemical compound [2H]C(Cl)(Cl)Cl HEDRZPFGACZZDS-MICDWDOJSA-N 0.000 description 1
- 230000009102 absorption Effects 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000003905 agrochemical Substances 0.000 description 1
- 239000008346 aqueous phase Substances 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical class BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 238000005285 chemical preparation method Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000001030 gas--liquid chromatography Methods 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 231100001225 mammalian toxicity Toxicity 0.000 description 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 238000005949 ozonolysis reaction Methods 0.000 description 1
- 150000004965 peroxy acids Chemical class 0.000 description 1
- 239000012071 phase Substances 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- CZDYPVPMEAXLPK-UHFFFAOYSA-N tetramethylsilane Chemical compound C[Si](C)(C)C CZDYPVPMEAXLPK-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C41/00—Preparation of ethers; Preparation of compounds having groups, groups or groups
- C07C41/48—Preparation of compounds having groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C43/00—Ethers; Compounds having groups, groups or groups
- C07C43/30—Compounds having groups
- C07C43/315—Compounds having groups containing oxygen atoms singly bound to carbon atoms not being acetal carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/02—Systems containing only non-condensed rings with a three-membered ring
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB7830371 | 1978-07-19 | ||
GB7830371 | 1978-07-19 |
Publications (1)
Publication Number | Publication Date |
---|---|
NL7905556A true NL7905556A (nl) | 1980-01-22 |
Family
ID=10498524
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
NL7905556A NL7905556A (nl) | 1978-07-19 | 1979-07-17 | Nieuw tussenprodukt bij de bereiding van esters van cyclopropaancarbonzuren en werkwijze ter bereiding van het tussenprodukt. |
Country Status (13)
-
1979
- 1979-07-17 CA CA331,953A patent/CA1123016A/en not_active Expired
- 1979-07-17 BE BE0/196342A patent/BE877749A/fr not_active IP Right Cessation
- 1979-07-17 IT IT24428/79A patent/IT1122205B/it active
- 1979-07-17 AU AU48984/79A patent/AU521243B2/en not_active Ceased
- 1979-07-17 DE DE19792928838 patent/DE2928838A1/de active Granted
- 1979-07-17 IL IL57821A patent/IL57821A/xx not_active IP Right Cessation
- 1979-07-17 DK DK300679A patent/DK300679A/da not_active Application Discontinuation
- 1979-07-17 IN IN516/DEL/79A patent/IN152614B/en unknown
- 1979-07-17 ZA ZA00793611A patent/ZA793611B/xx unknown
- 1979-07-17 FR FR7918459A patent/FR2431473A1/fr active Granted
- 1979-07-17 NL NL7905556A patent/NL7905556A/nl not_active Application Discontinuation
- 1979-07-17 JP JP8995079A patent/JPS5515487A/ja active Granted
- 1979-07-17 CH CH665079A patent/CH641136A5/de not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
FR2431473A1 (fr) | 1980-02-15 |
DE2928838A1 (de) | 1980-01-31 |
IL57821A (en) | 1982-01-31 |
CA1123016A (en) | 1982-05-04 |
IL57821A0 (en) | 1979-11-30 |
IN152614B (enrdf_load_stackoverflow) | 1984-02-25 |
DK300679A (da) | 1980-01-20 |
BE877749A (fr) | 1980-01-17 |
ZA793611B (en) | 1980-07-30 |
IT1122205B (it) | 1986-04-23 |
CH641136A5 (en) | 1984-02-15 |
DE2928838C2 (enrdf_load_stackoverflow) | 1988-01-21 |
JPS6217575B2 (enrdf_load_stackoverflow) | 1987-04-18 |
JPS5515487A (en) | 1980-02-02 |
IT7924428A0 (it) | 1979-07-17 |
FR2431473B1 (enrdf_load_stackoverflow) | 1981-11-13 |
AU521243B2 (en) | 1982-03-25 |
AU4898479A (en) | 1980-01-24 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
A85 | Still pending on 85-01-01 | ||
BA | A request for search or an international-type search has been filed | ||
BB | A search report has been drawn up | ||
BC | A request for examination has been filed | ||
BV | The patent application has lapsed |