HUP0004005A2 - Method for producing (+)-trans-chrysanthenum-monocarboxylic acid - Google Patents
Method for producing (+)-trans-chrysanthenum-monocarboxylic acidInfo
- Publication number
- HUP0004005A2 HUP0004005A2 HU0004005A HUP0004005A HUP0004005A2 HU P0004005 A2 HUP0004005 A2 HU P0004005A2 HU 0004005 A HU0004005 A HU 0004005A HU P0004005 A HUP0004005 A HU P0004005A HU P0004005 A2 HUP0004005 A2 HU P0004005A2
- Authority
- HU
- Hungary
- Prior art keywords
- trans
- monocarboxylic acid
- chrysanthenum
- producing
- production
- Prior art date
Links
- 238000004519 manufacturing process Methods 0.000 title abstract 4
- 150000003839 salts Chemical class 0.000 abstract 3
- VEMKTZHHVJILDY-UXHICEINSA-N bioresmethrin Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)OCC1=COC(CC=2C=CC=CC=2)=C1 VEMKTZHHVJILDY-UXHICEINSA-N 0.000 abstract 1
- XLOPRKKSAJMMEW-UHFFFAOYSA-N chrysanthemic acid Chemical compound CC(C)=CC1C(C(O)=O)C1(C)C XLOPRKKSAJMMEW-UHFFFAOYSA-N 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C61/00—Compounds having carboxyl groups bound to carbon atoms of rings other than six-membered aromatic rings
- C07C61/16—Unsaturated compounds
- C07C61/35—Unsaturated compounds having unsaturation outside the rings
- C07C61/37—Chrysanthemumic acid
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C211/00—Compounds containing amino groups bound to a carbon skeleton
- C07C211/01—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to acyclic carbon atoms
- C07C211/26—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to acyclic carbon atoms of an unsaturated carbon skeleton containing at least one six-membered aromatic ring
- C07C211/27—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to acyclic carbon atoms of an unsaturated carbon skeleton containing at least one six-membered aromatic ring having amino groups linked to the six-membered aromatic ring by saturated carbon chains
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/42—Separation; Purification; Stabilisation; Use of additives
- C07C51/43—Separation; Purification; Stabilisation; Use of additives by change of the physical state, e.g. crystallisation
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/42—Separation; Purification; Stabilisation; Use of additives
- C07C51/487—Separation; Purification; Stabilisation; Use of additives by treatment giving rise to chemical modification
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B2200/00—Indexing scheme relating to specific properties of organic compounds
- C07B2200/09—Geometrical isomers
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Crystallography & Structural Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
A találmány (+)-transz-krizantém-monokarbonsav és (S)-1-transz-1-fenil-2-metilpropilamin alkotta sóra, továbbá ennek a sónak azelőállítására, valamint ebből a sóból a (+)-transz-krizantém-monokarbonsav előállítására vonatkozik. A megoldás lényege, hogytetszőleges izomer összetételű krizantém-monokarbonsavból állíthatóelő a kívánt (+)-transz-krizantém-monokarbonsav, amely piretroidokelőállításánál értékes köztitermék. ÓThe invention relates to the salt formed by (+)-trans-chrysanthemum monocarboxylic acid and (S)-1-trans-1-phenyl-2-methylpropylamine, as well as to the production of this salt, and from this salt to (+)-trans-chrysanthemum monocarboxylic acid refers to its production. The essence of the solution is that the desired (+)-trans-chrysanthemum monocarboxylic acid can be produced from chrysanthemum monocarboxylic acid of any isomeric composition, which is a valuable intermediate in the production of pyrethroids. HE
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP29515499A JP4320870B2 (en) | 1999-10-18 | 1999-10-18 | (+)-Method for producing trans primary chrysanthemic acid |
Publications (3)
Publication Number | Publication Date |
---|---|
HU0004005D0 HU0004005D0 (en) | 2000-12-28 |
HUP0004005A2 true HUP0004005A2 (en) | 2001-11-28 |
HUP0004005A3 HUP0004005A3 (en) | 2003-10-28 |
Family
ID=17816966
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
HU0004005A HUP0004005A3 (en) | 1999-10-18 | 2000-10-13 | Method for producing (+)-trans-chrysanthenum-monocarboxylic acid |
Country Status (6)
Country | Link |
---|---|
JP (1) | JP4320870B2 (en) |
KR (1) | KR100645277B1 (en) |
CN (1) | CN1225452C (en) |
HU (1) | HUP0004005A3 (en) |
IN (1) | IN190898B (en) |
IT (1) | IT1320818B1 (en) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
ITMI20050231A1 (en) * | 2005-02-17 | 2006-08-18 | Endura Spa | PROCESS FOR OBTAINING ENANTIOMER OF CHRYSANTHEMICAL ACID |
CN101613268B (en) * | 2009-07-28 | 2012-06-13 | 大连凯飞化学股份有限公司 | Method for manufacturing rich reverse type first chrysanthemic acid |
CN101628206B (en) * | 2009-08-14 | 2012-04-04 | 德州中钿生物科技有限公司 | Nanofiltration membrane for removing gossypol in cottonseeds and method |
KR101856260B1 (en) | 2010-02-24 | 2018-05-09 | 치에시 파마슈티시 에스.피.아. | Process for production and purification of recombinant lysosomal alpha-mannosidase |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2721553B2 (en) * | 1989-08-11 | 1998-03-04 | 株式会社クラレ | Optical resolution of cis-trans mixed chrysanthemic acid |
US6268525B1 (en) * | 1998-01-29 | 2001-07-31 | Sumitomo Chemical Company, Limited | Process for producing optically active chrysanthemic acid |
US10079475B2 (en) * | 2014-05-19 | 2018-09-18 | Ngk Spark Plug Co., Ltd. | Plug connector, rubber member, and ring member |
-
1999
- 1999-10-18 JP JP29515499A patent/JP4320870B2/en not_active Expired - Fee Related
-
2000
- 2000-10-13 IN IN869MA2000 patent/IN190898B/en unknown
- 2000-10-13 HU HU0004005A patent/HUP0004005A3/en unknown
- 2000-10-16 CN CNB001342320A patent/CN1225452C/en not_active Expired - Fee Related
- 2000-10-16 IT IT2000TO000965A patent/IT1320818B1/en active
- 2000-10-17 KR KR1020000061007A patent/KR100645277B1/en not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
HU0004005D0 (en) | 2000-12-28 |
ITTO20000965A0 (en) | 2000-10-16 |
JP4320870B2 (en) | 2009-08-26 |
IT1320818B1 (en) | 2003-12-10 |
KR100645277B1 (en) | 2006-11-13 |
ITTO20000965A1 (en) | 2002-04-16 |
HUP0004005A3 (en) | 2003-10-28 |
JP2001114728A (en) | 2001-04-24 |
CN1298862A (en) | 2001-06-13 |
CN1225452C (en) | 2005-11-02 |
IN190898B (en) | 2003-08-30 |
KR20010070144A (en) | 2001-07-25 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
FD9A | Lapse of provisional protection due to non-payment of fees |