UA111142C2 - Одержання заміщених похідних 2-фторакрилової кислоти - Google Patents
Одержання заміщених похідних 2-фторакрилової кислотиInfo
- Publication number
- UA111142C2 UA111142C2 UAA201200780A UAA201200780A UA111142C2 UA 111142 C2 UA111142 C2 UA 111142C2 UA A201200780 A UAA201200780 A UA A201200780A UA A201200780 A UAA201200780 A UA A201200780A UA 111142 C2 UA111142 C2 UA 111142C2
- Authority
- UA
- Ukraine
- Prior art keywords
- substituted
- acid derivatives
- fluoracrylic acid
- fluoracrylic
- production
- Prior art date
Links
- TYCFGHUTYSLISP-UHFFFAOYSA-N 2-fluoroprop-2-enoic acid Chemical class data:image/svg+xml;base64,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 data:image/svg+xml;base64,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 OC(=O)C(F)=C TYCFGHUTYSLISP-UHFFFAOYSA-N 0.000 title abstract 2
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/62—Halogen-containing esters
- C07C69/65—Halogen-containing esters of unsaturated acids
- C07C69/653—Acrylic acid esters; Methacrylic acid esters; Haloacrylic acid esters; Halomethacrylic acid esters
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C67/00—Preparation of carboxylic acid esters
- C07C67/30—Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group
- C07C67/307—Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group by introduction of halogen; by substitution of halogen atoms by other halogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C67/00—Preparation of carboxylic acid esters
- C07C67/30—Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group
- C07C67/317—Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group by splitting-off hydrogen or functional groups; by hydrogenolysis of functional groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/62—Halogen-containing esters
- C07C69/63—Halogen-containing esters of saturated acids
Abstract
Винахід належить до способу одержання заміщених похідних 2-фторакрилової кислоти.
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE102009030681A DE102009030681A1 (de) | 2009-06-26 | 2009-06-26 | Herstellung von substituierten 2-Fluoracrylsäurederivaten |
PCT/EP2010/058870 WO2010149683A1 (de) | 2009-06-26 | 2010-06-23 | Herstellung von substituierten 2-fluoracrylsäurederivaten |
Publications (1)
Publication Number | Publication Date |
---|---|
UA111142C2 true UA111142C2 (uk) | 2016-04-11 |
Family
ID=42697225
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
UAA201200780A UA111142C2 (uk) | 2009-06-26 | 2010-06-23 | Одержання заміщених похідних 2-фторакрилової кислоти |
Country Status (12)
Country | Link |
---|---|
US (1) | US9000210B2 (uk) |
EP (1) | EP2445862B1 (uk) |
JP (1) | JP5628305B2 (uk) |
KR (1) | KR101364292B1 (uk) |
CN (1) | CN102459143B (uk) |
CA (1) | CA2765897C (uk) |
DE (1) | DE102009030681A1 (uk) |
ES (1) | ES2699825T3 (uk) |
IL (1) | IL217001A (uk) |
RU (1) | RU2553990C2 (uk) |
UA (1) | UA111142C2 (uk) |
WO (1) | WO2010149683A1 (uk) |
Families Citing this family (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP5521640B2 (ja) * | 2009-05-19 | 2014-06-18 | セントラル硝子株式会社 | 2−フルオロアクリル酸エステルの製造方法 |
CN102211999A (zh) * | 2011-05-25 | 2011-10-12 | 原平市同利化工有限责任公司 | 2-氟代丙烯酸烷基酯的制备方法 |
BR112017007509B1 (pt) * | 2014-10-14 | 2021-02-02 | Syngenta Participations Ag | processo para a preparação de 1-(3,5-dicloro-4-fluorofenil)-2,2,2-trifluoro-etanona |
JP6160651B2 (ja) | 2015-04-09 | 2017-07-12 | ダイキン工業株式会社 | アクリル酸誘導体含有組成物、及びアクリル酸誘導体の安定化方法 |
JP6202037B2 (ja) | 2015-04-09 | 2017-09-27 | ダイキン工業株式会社 | 組成物 |
CN113773198A (zh) | 2015-04-09 | 2021-12-10 | 大金工业株式会社 | 含有丙烯酸衍生物的组合物和丙烯酸衍生物的稳定化方法 |
CN107848944B (zh) * | 2015-08-07 | 2021-01-15 | 大金工业株式会社 | 水除去方法 |
WO2017026423A1 (ja) | 2015-08-07 | 2017-02-16 | ダイキン工業株式会社 | アクリル酸誘導体の精製方法 |
US10252971B2 (en) | 2015-08-27 | 2019-04-09 | AGC Inc. | Method for producing halogenated acrylic acid derivative |
WO2021191876A1 (en) | 2020-03-27 | 2021-09-30 | Vifor (International) Ltd. | Synthesis of methyl 2-fluoroacrylate |
WO2021215450A1 (ja) * | 2020-04-20 | 2021-10-28 | ダイキン工業株式会社 | α-フルオロアクリル酸エステルの製造方法 |
WO2021215452A1 (ja) * | 2020-04-20 | 2021-10-28 | ダイキン工業株式会社 | α-フルオロアクリル酸エステルの製造方法 |
Family Cites Families (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2245547A (en) * | 1939-10-19 | 1941-06-10 | Pittsburgh Plate Glass Co | Method of preparing halo acrylic esters |
SU380637A1 (ru) * | 1971-02-22 | 1973-05-15 | Ордена Трудового Красного Знамени институт органической , физической химии А. Е. Арбузова | СПОСОБ ПОЛУЧЕНИЯ МОНО- ИЛИ ДИ-а-ФТОРАКРИЛАТОВ |
JPS6078943A (en) * | 1983-10-07 | 1985-05-04 | Daikin Ind Ltd | Production of alpha-fluoroacrylic acid ester |
JPH0150690B2 (uk) * | 1983-10-07 | 1989-10-31 | Daikin Kogyo Co Ltd | |
DE3928990A1 (de) | 1989-09-01 | 1991-03-07 | Bayer Ag | Verfahren zur herstellung von (alpha)-fluoroacrylsaeurederivaten |
JP2001172223A (ja) | 1999-12-17 | 2001-06-26 | Nippon Mektron Ltd | 2−フルオロアクリル酸またはそのエステルの製造法 |
JP2003212821A (ja) * | 2002-01-17 | 2003-07-30 | Nippon Shokubai Co Ltd | (メタ)アクリル酸系モノマーの重合防止方法 |
CN101312938B (zh) * | 2005-11-21 | 2011-09-28 | 东亚合成株式会社 | (甲基)丙烯酸酯的制造方法 |
-
2009
- 2009-06-26 DE DE102009030681A patent/DE102009030681A1/de not_active Ceased
-
2010
- 2010-06-23 CA CA2765897A patent/CA2765897C/en active Active
- 2010-06-23 EP EP10725781.8A patent/EP2445862B1/de active Active
- 2010-06-23 JP JP2012516705A patent/JP5628305B2/ja active Active
- 2010-06-23 RU RU2012102458/04A patent/RU2553990C2/ru active
- 2010-06-23 UA UAA201200780A patent/UA111142C2/uk unknown
- 2010-06-23 ES ES10725781T patent/ES2699825T3/es active Active
- 2010-06-23 WO PCT/EP2010/058870 patent/WO2010149683A1/de active Application Filing
- 2010-06-23 US US13/379,062 patent/US9000210B2/en active Active
- 2010-06-23 CN CN201080028159.4A patent/CN102459143B/zh active Active
- 2010-06-23 KR KR1020127001903A patent/KR101364292B1/ko active IP Right Grant
-
2011
- 2011-12-15 IL IL217001A patent/IL217001A/en active IP Right Grant
Also Published As
Publication number | Publication date |
---|---|
CA2765897A1 (en) | 2010-12-23 |
CN102459143A (zh) | 2012-05-16 |
EP2445862B1 (de) | 2018-09-05 |
US9000210B2 (en) | 2015-04-07 |
KR20120034113A (ko) | 2012-04-09 |
IL217001D0 (en) | 2012-02-29 |
DE102009030681A1 (de) | 2010-12-30 |
JP2012530756A (ja) | 2012-12-06 |
JP5628305B2 (ja) | 2014-11-19 |
ES2699825T3 (es) | 2019-02-13 |
RU2553990C2 (ru) | 2015-06-20 |
KR101364292B1 (ko) | 2014-02-18 |
EP2445862A1 (de) | 2012-05-02 |
CA2765897C (en) | 2016-05-10 |
WO2010149683A1 (de) | 2010-12-29 |
RU2012102458A (ru) | 2013-08-10 |
IL217001A (en) | 2015-09-24 |
US20120283468A1 (en) | 2012-11-08 |
CN102459143B (zh) | 2015-09-30 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
UA111142C2 (uk) | Одержання заміщених похідних 2-фторакрилової кислоти | |
SMT201600011B (it) | Composti per ridurre la produzione di beta-amiloide | |
CL2009000503A1 (es) | Proceso de preparacion de compuestos derivados de acido 2-amino-5-cianobenzoico-3-sustituidos o 1h-pirazol-5-carboxamida. | |
SG178239A1 (en) | Process for the preparation of derivatives of 1-(2-halobiphenyl-4-yl)-cyclopropanecarboxylic acid | |
CR20130625A (es) | Derivados de la piperidina 3-espirocíclica como agonistas de receptores de la ghrelina | |
ME02348B (me) | POSTUPAK ZA PRIPREMU ESTARA (5-FLUORO-2-METIL-3-HINOLIN-2-lL METIL-INDOL-1-IL)-SIRĆETNE KISELINE | |
CL2011000296A1 (es) | Proceso de preparación del ester metílico del ácido 4-oxo-octahidro-indol-1-carboxílico y compuestos intermediarios utilizados. | |
UA112539C2 (uk) | Спосіб одержання похідних 2-карбоксамідциклоаміносечовини | |
EA201290165A1 (ru) | Способ получения производного фенилаланина | |
UA106886C2 (uk) | Спосіб одержання 1-бензил-3-гідроксиметил-1h-індазолу і його похідних та проміжні сполуки магнію | |
MX2012010443A (es) | Proceso para la preparacion de 1-alquiltetrazoles 5-sustituidos. | |
EA201270343A1 (ru) | Фотохимический способ получения артемисинина | |
IL227590D0 (en) | A method for producing a history of 1-h-pyrrolidine-4,2-deion | |
IN2014DN09451A (uk) | ||
BRPI0913890A2 (pt) | Método para produção de ácido 3-metil-2tiofenocarboxílico | |
CR20150028A (es) | Derivados de ariletinilo | |
CR20140531A (es) | Derivados de ariletinilo | |
GT201300078A (es) | Proceso para la preparacion de inhibidores de pan-cdk de la formula ( i ), e intermediarios de la preparacion | |
MX345822B (es) | Separacion de enantiomeros derivados de triazina usando acido tartarico. | |
DK2457921T3 (da) | Aureolinsyre-derivater, en fremgangsmåde til fremstilling deraf samt anvendelser deraf | |
MX361998B (es) | Procedimiento de preparacion de derivados de acido 4-haloalquil-3-mercapto-2 sustituido-hidroxibenzoico. | |
BR112014001382A2 (pt) | método de produção de composto derivado do ácido c4 | |
BRPI1012010A2 (pt) | método de produção de ácido succínico | |
CY1117823T1 (el) | Μεθοδος για την παρασκευη κρυσταλλικης μορφης ι της αγομελατινης | |
MX2013002395A (es) | Procedimiento de preparacion de ditiin-tetracarboximidas. |