ES2058907T3 - Procedimiento para la sintesis de 9,9-bis(4-hidroxifenil)fluoreno. - Google Patents
Procedimiento para la sintesis de 9,9-bis(4-hidroxifenil)fluoreno.Info
- Publication number
- ES2058907T3 ES2058907T3 ES90906045T ES90906045T ES2058907T3 ES 2058907 T3 ES2058907 T3 ES 2058907T3 ES 90906045 T ES90906045 T ES 90906045T ES 90906045 T ES90906045 T ES 90906045T ES 2058907 T3 ES2058907 T3 ES 2058907T3
- Authority
- ES
- Spain
- Prior art keywords
- pct
- fluorene
- raw product
- sec
- dissolved
- Prior art date
- Legal status (The legal status 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 status listed.)
- Expired - Lifetime
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C39/00—Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a six-membered aromatic ring
- C07C39/12—Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a six-membered aromatic ring polycyclic with no unsaturation outside the aromatic rings
- C07C39/17—Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a six-membered aromatic ring polycyclic with no unsaturation outside the aromatic rings containing other rings in addition to the six-membered aromatic rings, e.g. cyclohexylphenol
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C37/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring
- C07C37/11—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring by reactions increasing the number of carbon atoms
- C07C37/20—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring by reactions increasing the number of carbon atoms using aldehydes or ketones
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2603/00—Systems containing at least three condensed rings
- C07C2603/02—Ortho- or ortho- and peri-condensed systems
- C07C2603/04—Ortho- or ortho- and peri-condensed systems containing three rings
- C07C2603/06—Ortho- or ortho- and peri-condensed systems containing three rings containing at least one ring with less than six ring members
- C07C2603/10—Ortho- or ortho- and peri-condensed systems containing three rings containing at least one ring with less than six ring members containing five-membered rings
- C07C2603/12—Ortho- or ortho- and peri-condensed systems containing three rings containing at least one ring with less than six ring members containing five-membered rings only one five-membered ring
- C07C2603/18—Fluorenes; Hydrogenated fluorenes
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Abstract
PROCEDIMIENTO PARA LA SINTESIS DE 9,9-BIS(4-HIDROXIFENIL)FLUORENO CON FENOL EN EXCESO, POR MEDIO DE UN CATALIZADOR LIQUIDO, PARA CUYA PRODUCCION SE DISUELVE TRICLORURO DE ALUMINIO EN UN DISOLVENTE ORGANICO LIBRE DE AGUA, TAL COMO TOLUENO, QUE TIENE PROPIEDADES DE DONANTE DE ELECTRONES, CON ENTRADA SIMULTANEA DE GAS DE CLORURO DE HIDROGENO. PARA LA SINTESIS SE DISUELVE LA FLUORENONA, POR EJEMPLO A 60 (GRADOS) C, EN EL FENOL LIQUIDO, A CONTINUACION DE LO CUAL SE AÑADE EL CATALIZADOR, POR GOTEO Y BAJO AGITACION, EN UNA CANTIDAD TAL QUE LA TEMPERATURA DE LA MEZCLA REACTIVA SE MANTENGA POR DEBAJO DE 60 (GRADOS) C. FINALIZADA LA ADICION DE CATALIZADOR Y DESPUES DE UN TIEMPO DE REPOSO DE VARIAS HORAS, EL PRODUCTO EN CRUDO SE TRATA CON AGUA CALIENTE Y SE ELIMINA EL FENOL EN EXCESO POR DESTILACION. SE VUELVE A LAVAR CON AGUA CALIENTE Y SE DISUELVE EN ACETONA CALIENTE, SE DEJA CRISTALIZAR, SE FILTRA Y SE SECA AL VACIO. FINALMENTE, EL PRODUCTO EN CRUDO SE RECRISTALIZA EN 1,2-DICLOROETANO.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AT901/89A AT393502B (de) | 1989-04-17 | 1989-04-17 | Verfahren zur synthese von 9,9-bis(4-hydroxyphenyl)fluoren |
Publications (1)
Publication Number | Publication Date |
---|---|
ES2058907T3 true ES2058907T3 (es) | 1994-11-01 |
Family
ID=3502450
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ES90906045T Expired - Lifetime ES2058907T3 (es) | 1989-04-17 | 1990-04-17 | Procedimiento para la sintesis de 9,9-bis(4-hidroxifenil)fluoreno. |
Country Status (9)
Country | Link |
---|---|
US (1) | US5110994A (es) |
EP (1) | EP0419631B1 (es) |
JP (1) | JPH03505464A (es) |
AT (2) | AT393502B (es) |
CA (1) | CA2030539A1 (es) |
DE (1) | DE59001776D1 (es) |
DK (1) | DK0419631T3 (es) |
ES (1) | ES2058907T3 (es) |
WO (1) | WO1990012776A1 (es) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP3039048B2 (ja) * | 1991-11-01 | 2000-05-08 | 住友化学工業株式会社 | ポジ型感放射線性レジスト組成物 |
US5304688A (en) * | 1993-04-13 | 1994-04-19 | The Dow Chemical Company | Process for the preparation of bishydroxy aromatic compounds |
ITSV20010013A1 (it) | 2001-04-24 | 2002-10-24 | Ferrania Spa | 9,9-bis-(4-idrossifenil)-fluorene ad alta purezza e metodo perla sua preparazione e purificazione |
CN100436391C (zh) * | 2006-12-20 | 2008-11-26 | 哈尔滨工程大学 | 磁性固体超强酸催化合成双酚芴的方法 |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2775620A (en) * | 1954-07-12 | 1956-12-25 | Shell Dev | Production of bis (hydroxyaryl) substituted compounds |
DE2508710A1 (de) * | 1975-02-28 | 1976-09-09 | Bayer Ag | 1,1,2-tris-(p-hydroxyphenyl)-1- phenyl-aethane sowie ein verfahren zu ihrer herstellung |
US4024194A (en) * | 1976-03-16 | 1977-05-17 | General Electric Company | Process for the purification of 9,9-bis(4-hydroxyphenyl)-fluorene |
US4049721A (en) * | 1976-09-07 | 1977-09-20 | General Electric Company | Purification of crude 9,9-bis-(4-hydroxyphenyl)-fluorene |
EP0065060B1 (de) * | 1981-05-07 | 1987-01-07 | ISOVOLTAÖsterreichische IsolierstoffwerkeAktiengesellschaft | Verfahren zur Herstellung von Phenol-Keton-Kondensationsprodukten, insbesondere von Diphenolen |
DE3439484A1 (de) * | 1984-10-27 | 1986-05-07 | Röhm GmbH, 6100 Darmstadt | Verfahren zur herstellung von 9,9-bis-(4-hydroxyphenyl)-fluoren |
-
1989
- 1989-04-17 AT AT901/89A patent/AT393502B/de not_active IP Right Cessation
-
1990
- 1990-04-17 EP EP90906045A patent/EP0419631B1/de not_active Expired - Lifetime
- 1990-04-17 US US07/613,668 patent/US5110994A/en not_active Expired - Fee Related
- 1990-04-17 WO PCT/AT1990/000031 patent/WO1990012776A1/de active IP Right Grant
- 1990-04-17 DE DE9090906045T patent/DE59001776D1/de not_active Expired - Fee Related
- 1990-04-17 JP JP2505895A patent/JPH03505464A/ja active Pending
- 1990-04-17 CA CA002030539A patent/CA2030539A1/en not_active Abandoned
- 1990-04-17 ES ES90906045T patent/ES2058907T3/es not_active Expired - Lifetime
- 1990-04-17 AT AT90906045T patent/ATE90661T1/de not_active IP Right Cessation
- 1990-04-17 DK DK90906045.1T patent/DK0419631T3/da not_active Application Discontinuation
Also Published As
Publication number | Publication date |
---|---|
US5110994A (en) | 1992-05-05 |
DK0419631T3 (da) | 1993-10-04 |
ATE90661T1 (de) | 1993-07-15 |
AT393502B (de) | 1991-11-11 |
WO1990012776A1 (de) | 1990-11-01 |
EP0419631B1 (de) | 1993-06-16 |
DE59001776D1 (de) | 1993-07-22 |
CA2030539A1 (en) | 1990-10-18 |
JPH03505464A (ja) | 1991-11-28 |
EP0419631A1 (de) | 1991-04-03 |
ATA90189A (de) | 1991-04-15 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
FG2A | Definitive protection |
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