PL442918A1 - Sposób wydzielania z mieszaniny poreakcyjnej 4-chloro-2-metylofenoksyoctanów n-bromoalkilowych techniką chromatografii typu Flash - Google Patents
Sposób wydzielania z mieszaniny poreakcyjnej 4-chloro-2-metylofenoksyoctanów n-bromoalkilowych techniką chromatografii typu FlashInfo
- Publication number
- PL442918A1 PL442918A1 PL442918A PL44291822A PL442918A1 PL 442918 A1 PL442918 A1 PL 442918A1 PL 442918 A PL442918 A PL 442918A PL 44291822 A PL44291822 A PL 44291822A PL 442918 A1 PL442918 A1 PL 442918A1
- Authority
- PL
- Poland
- Prior art keywords
- chloro
- reaction mixture
- bromoalkyl
- methylphenoxyacetates
- isolating
- Prior art date
Links
- 238000000034 method Methods 0.000 title abstract 4
- WHKUVVPPKQRRBV-UHFFFAOYSA-N Trasan Chemical class CC1=CC(Cl)=CC=C1OCC(O)=O WHKUVVPPKQRRBV-UHFFFAOYSA-N 0.000 title abstract 2
- 238000003818 flash chromatography Methods 0.000 title abstract 2
- 239000012451 post-reaction mixture Substances 0.000 title abstract 2
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 abstract 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 abstract 3
- SODPIMGUZLOIPE-UHFFFAOYSA-N (4-chlorophenoxy)acetic acid Chemical compound OC(=O)COC1=CC=C(Cl)C=C1 SODPIMGUZLOIPE-UHFFFAOYSA-N 0.000 abstract 1
- 229920000742 Cotton Polymers 0.000 abstract 1
- 230000015572 biosynthetic process Effects 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- IJKVHSBPTUYDLN-UHFFFAOYSA-N dihydroxy(oxo)silane Chemical compound O[Si](O)=O IJKVHSBPTUYDLN-UHFFFAOYSA-N 0.000 abstract 1
- 239000003480 eluent Substances 0.000 abstract 1
- 150000002148 esters Chemical class 0.000 abstract 1
- 239000007788 liquid Substances 0.000 abstract 1
- 239000011541 reaction mixture Substances 0.000 abstract 1
- 239000004576 sand Substances 0.000 abstract 1
- 238000000926 separation method Methods 0.000 abstract 1
- 239000007787 solid Substances 0.000 abstract 1
- 238000003786 synthesis reaction Methods 0.000 abstract 1
Classifications
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N30/00—Investigating or analysing materials by separation into components using adsorption, absorption or similar phenomena or using ion-exchange, e.g. chromatography or field flow fractionation
- G01N30/02—Column chromatography
-
- 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
- A01N39/00—Biocides, pest repellants or attractants, or plant growth regulators containing aryloxy- or arylthio-aliphatic or cycloaliphatic compounds, containing the group or, e.g. phenoxyethylamine, phenylthio-acetonitrile, phenoxyacetone
- A01N39/02—Aryloxy-carboxylic acids; Derivatives thereof
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C59/00—Compounds having carboxyl groups bound to acyclic carbon atoms and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups
- C07C59/40—Unsaturated compounds
- C07C59/58—Unsaturated compounds containing ether groups, groups, groups, or groups
- C07C59/64—Unsaturated compounds containing ether groups, groups, groups, or groups containing six-membered aromatic rings
- C07C59/66—Unsaturated compounds containing ether groups, groups, groups, or groups containing six-membered aromatic rings the non-carboxylic part of the ether containing six-membered aromatic rings
- C07C59/68—Unsaturated compounds containing ether groups, groups, groups, or groups containing six-membered aromatic rings the non-carboxylic part of the ether containing six-membered aromatic rings the oxygen atom of the ether group being bound to a non-condensed six-membered aromatic ring
- C07C59/70—Ethers of hydroxy-acetic acid, e.g. substitutes on the ring
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Health & Medical Sciences (AREA)
- Biochemistry (AREA)
- Pest Control & Pesticides (AREA)
- General Physics & Mathematics (AREA)
- Immunology (AREA)
- Pathology (AREA)
- Analytical Chemistry (AREA)
- Agronomy & Crop Science (AREA)
- Physics & Mathematics (AREA)
- Plant Pathology (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Przedmiotem zgłoszenia jest sposób wydzielania z mieszaniny poreakcyjnej 4-chloro-2-metylofenoksyoctanów n-bromoalkilowych techniką chromatografii typu Flash. W sposobie tym mieszaninę proreakcyjną z procesu syntezy n-bromoalkilowych estrów kwasu 4-chloro-2-fenoksyoctowego o wzorze ogólnym 1, gdzie R oznacza podstawnik alkilowy zawierający od czterech do dwunastu atomów węgla poddaje się rozdziałowi z użyciem kolumny chromatograficznej o regulowanym przepływie, wypełnionej fazą stałą w postaci żelu krzemionkowego 60 o wielkości ziarna 70 - 230 mesh, zabezpieczoną wacikiem i pokrytej warstwą piasku, przy wykorzystaniu jako eluentu roztworu octanu etylu w heksanie o stężeniu od 10% do 30%, przy czym rozdział przeprowadza się w nadciśnieniu 0,4 bar względem ciśnienia atmosferycznego, przy przepływie cieczy ok. 5 cm/min.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
PL442918A PL442918A1 (pl) | 2022-11-23 | 2022-11-23 | Sposób wydzielania z mieszaniny poreakcyjnej 4-chloro-2-metylofenoksyoctanów n-bromoalkilowych techniką chromatografii typu Flash |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
PL442918A PL442918A1 (pl) | 2022-11-23 | 2022-11-23 | Sposób wydzielania z mieszaniny poreakcyjnej 4-chloro-2-metylofenoksyoctanów n-bromoalkilowych techniką chromatografii typu Flash |
Publications (1)
Publication Number | Publication Date |
---|---|
PL442918A1 true PL442918A1 (pl) | 2024-03-11 |
Family
ID=90195168
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PL442918A PL442918A1 (pl) | 2022-11-23 | 2022-11-23 | Sposób wydzielania z mieszaniny poreakcyjnej 4-chloro-2-metylofenoksyoctanów n-bromoalkilowych techniką chromatografii typu Flash |
Country Status (1)
Country | Link |
---|---|
PL (1) | PL442918A1 (pl) |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB573510A (en) * | 1943-08-30 | 1945-11-23 | Reginald Thomas Foster | Improvements in or relating to the production of chloroaryloxyalkylcarboxylic compounds |
GB729625A (en) * | 1952-05-29 | 1955-05-11 | Konink Ind Mij Voorheen Noury | Improvements in or relating to the preparation of non-odorous 2-methyl-4-chlorophenoxyacetic acid and its application as a selective weed-killer |
CH507893A (de) * | 1968-09-26 | 1971-05-31 | Spolana Np | Verfahren zur Herstellung von Estern herbizider Phenoxyalkylcarbonsäuren |
CN101921190A (zh) * | 2010-09-01 | 2010-12-22 | 江苏好收成韦恩农化股份有限公司 | 生产2-甲基-4-氯苯氧乙酸的酯类的方法 |
PL437423A1 (pl) * | 2021-03-26 | 2022-10-03 | Politechnika Poznańska | Nowe n-bromoalkilowe estry kwasu 4-chloro-2-fenoksyoctowego, sposób ich otrzymywania oraz ich zastosowanie |
-
2022
- 2022-11-23 PL PL442918A patent/PL442918A1/pl unknown
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB573510A (en) * | 1943-08-30 | 1945-11-23 | Reginald Thomas Foster | Improvements in or relating to the production of chloroaryloxyalkylcarboxylic compounds |
GB729625A (en) * | 1952-05-29 | 1955-05-11 | Konink Ind Mij Voorheen Noury | Improvements in or relating to the preparation of non-odorous 2-methyl-4-chlorophenoxyacetic acid and its application as a selective weed-killer |
CH507893A (de) * | 1968-09-26 | 1971-05-31 | Spolana Np | Verfahren zur Herstellung von Estern herbizider Phenoxyalkylcarbonsäuren |
CN101921190A (zh) * | 2010-09-01 | 2010-12-22 | 江苏好收成韦恩农化股份有限公司 | 生产2-甲基-4-氯苯氧乙酸的酯类的方法 |
PL437423A1 (pl) * | 2021-03-26 | 2022-10-03 | Politechnika Poznańska | Nowe n-bromoalkilowe estry kwasu 4-chloro-2-fenoksyoctowego, sposób ich otrzymywania oraz ich zastosowanie |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Jovel et al. | A selective and practical synthesis of nitroolefins | |
IN2014DN02166A (pl) | ||
US20080280859A1 (en) | Gemini vitamin d3 compounds and methods of use thereof | |
PL442918A1 (pl) | Sposób wydzielania z mieszaniny poreakcyjnej 4-chloro-2-metylofenoksyoctanów n-bromoalkilowych techniką chromatografii typu Flash | |
Xu et al. | Efficient synthesis of furoquinolinones using Hendrickson reagent-initiated cascade annulation | |
US20210355099A1 (en) | Highly efficient synthesis of z-macrocycles using stereoretentive, ruthenium-based metathesis catalysts | |
Panchaud et al. | 3‐Pyridinesulfonyl Azide: A Useful Reagent for Radical Azidation | |
Seitz et al. | Vic-tricarbonyl compounds: synthesis of (±)-9-epi-Wailupemycin A | |
Yadav et al. | Ultrasound-accelerated synthesis of chiral allylic alcohols promoted by indium metal | |
Kobayashi et al. | Total synthesis of (−)-phaeosphaeride B by a biomimetic conversion from (−)-phaeosphaeride A | |
CN106831765B (zh) | 2-(2,6-二氰基苯基)咪唑并[1,2-α]吡啶类化合物及其制备方法 | |
Vostrikov et al. | A new approach to the synthesis of cross-conjugated cyclopentenone prostaglandins. Synthesis of (±)-15-deoxy-Δ12, 14-prostaglandin J2 methyl ester | |
Churches et al. | Stereoselectivity of the Petasis reaction with various chiral amines and styrenylboronic acids | |
Koc et al. | Total syntheses of heliotridane and pseudoheliotridane through nitrodiene–acrylate 6π-electrocyclization/[3+ 2] cycloaddition | |
WO2018220730A1 (ja) | Pge1コアブロック誘導体およびその製造方法 | |
Xu et al. | A new route to fluorine-containing aziridines and α-amino esters | |
WO2012111025A4 (en) | 1,2,3-triazole containing artemisinin compounds and process for preparation thereof | |
Di Bussolo et al. | Aminolysis of glycal-derived allyl epoxides and activated aziridines. Effects of the absence of coordination processes on the regio-and stereoselectivity | |
Hamberg | Resolution of stereoisomers of ω2-hydroxy acids and 2-alkanols by gas-liquid chromatography | |
WO2016164565A1 (en) | Trans-cycloheptenes and hetero-trans-cycloheptenes for bioorthogonal coupling | |
CN104356082B (zh) | 一类取代杂环衍生物及其制备方法 | |
Ghanty et al. | Stereoselective syntheses of siphonarienal and siphonarienone | |
ATE404549T1 (de) | Neue pharmakologisch aktive dauerpheromonverbindung zur steuerung von alterung und stress sowie verfahren zu deren isolierung und kennzeichnung | |
Mohapatra et al. | Highly selective approach for the total synthesis of (+)-heliconol A | |
Jung et al. | Synthesis of BCD tricyclic analogues of the novel cardiac glycoside rhodexin A |