JP2006117673A - シクロブタンテトラカルボキシレート化合物及びその製造方法 - Google Patents
シクロブタンテトラカルボキシレート化合物及びその製造方法 Download PDFInfo
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- JP2006117673A JP2006117673A JP2005303996A JP2005303996A JP2006117673A JP 2006117673 A JP2006117673 A JP 2006117673A JP 2005303996 A JP2005303996 A JP 2005303996A JP 2005303996 A JP2005303996 A JP 2005303996A JP 2006117673 A JP2006117673 A JP 2006117673A
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- -1 Cyclobutanetetracarboxylate compound Chemical class 0.000 title claims abstract description 11
- 238000004519 manufacturing process Methods 0.000 title abstract description 9
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims abstract description 9
- 239000002904 solvent Substances 0.000 claims abstract description 9
- 150000001875 compounds Chemical class 0.000 claims abstract description 8
- 125000000962 organic group Chemical group 0.000 claims abstract description 7
- 230000002378 acidificating effect Effects 0.000 claims abstract description 5
- 238000005886 esterification reaction Methods 0.000 claims abstract description 5
- 229910052736 halogen Inorganic materials 0.000 claims abstract description 3
- 150000002367 halogens Chemical class 0.000 claims abstract description 3
- 150000002431 hydrogen Chemical class 0.000 claims abstract description 3
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 3
- 239000001257 hydrogen Substances 0.000 claims abstract description 3
- 230000001678 irradiating effect Effects 0.000 claims abstract description 3
- 239000002243 precursor Substances 0.000 claims abstract description 3
- 238000007363 ring formation reaction Methods 0.000 claims abstract description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 15
- 238000000034 method Methods 0.000 claims description 13
- 238000006243 chemical reaction Methods 0.000 claims description 9
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical group CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 claims description 6
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims description 4
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 claims description 4
- 239000000203 mixture Substances 0.000 claims description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 3
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 2
- 125000004122 cyclic group Chemical group 0.000 claims description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 2
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims description 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 2
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 claims description 2
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 2
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 230000032050 esterification Effects 0.000 abstract 1
- YGYCECQIOXZODZ-UHFFFAOYSA-N 4415-87-6 Chemical compound O=C1OC(=O)C2C1C1C(=O)OC(=O)C12 YGYCECQIOXZODZ-UHFFFAOYSA-N 0.000 description 7
- DKXPPORBGHZJHX-UHFFFAOYSA-N cyclobutane-1,1,2,2-tetracarboxylic acid Chemical compound OC(=O)C1(C(O)=O)CCC1(C(O)=O)C(O)=O DKXPPORBGHZJHX-UHFFFAOYSA-N 0.000 description 5
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 3
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 3
- CURBACXRQKTCKZ-UHFFFAOYSA-N cyclobutane-1,2,3,4-tetracarboxylic acid Chemical compound OC(=O)C1C(C(O)=O)C(C(O)=O)C1C(O)=O CURBACXRQKTCKZ-UHFFFAOYSA-N 0.000 description 3
- LDCRTTXIJACKKU-ONEGZZNKSA-N dimethyl fumarate Chemical compound COC(=O)\C=C\C(=O)OC LDCRTTXIJACKKU-ONEGZZNKSA-N 0.000 description 2
- 229960004419 dimethyl fumarate Drugs 0.000 description 2
- 239000001530 fumaric acid Substances 0.000 description 2
- 150000007522 mineralic acids Chemical class 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 238000000967 suction filtration Methods 0.000 description 2
- NXMOMNBIDWYNOP-UHFFFAOYSA-N tetramethyl cyclobutane-1,2,3,4-tetracarboxylate Chemical compound COC(=O)C1C(C(=O)OC)C(C(=O)OC)C1C(=O)OC NXMOMNBIDWYNOP-UHFFFAOYSA-N 0.000 description 2
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 2
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000004075 alteration Effects 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical group CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 230000037361 pathway Effects 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 230000002194 synthesizing effect Effects 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/74—Esters of carboxylic acids having an esterified carboxyl group bound to a carbon atom of a ring other than a six-membered aromatic ring
-
- 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
- C07C67/333—Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group by isomerisation; by change of size of the carbon skeleton
- C07C67/343—Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms
- C07C67/347—Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms by addition to unsaturated carbon-to-carbon bonds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/04—Systems containing only non-condensed rings with a four-membered ring
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
Abstract
Description
(a)次の一般式(II):
(b)一般式(IV)で表される前駆体化合物にエネルギー線を照射して環化反応を行って一般式(I)で表されるシクロブタンテトラカルボキシレート化合物を得ることを含む。
5リットルのフラスコに、メタノール(3000mL、75mol)、次いでフマル酸(1160g、10mol)及び濃硫酸(10mL、0.2mol)を加えた。反応は温度を75℃に制御して10時間行い、次いで室温まで冷却した。得られた固体を吸引濾過により回収し、メタノールで洗浄し、フマル酸ジメチル(1224g、8.5mol)を得た。
Claims (12)
- 前記一価の有機基が直鎖状、分枝状又は環状のC1〜C4アルキルである、請求項1に記載のシクロブタンテトラカルボキシレート化合物。
- 前記一価の有機基がメチル、エチル、プロピル、イソプロピル、ブチル又はイソブチルである、請求項1に記載のシクロブタンテトラカルボキシレート化合物。
- 一般式(III)で表されるアルコールがメタノール、エタノール、プロパノール又はイソプロパノールである、請求項4に記載の方法。
- 工程(a)の反応が60〜110℃の温度で行われる、請求項4に記載の方法。
- 工程(a)の反応が2〜20時間行われる、請求項4に記載の方法。
- 工程(b)に用いられるエネルギー線が200〜600nmの波長を有する光源である、請求項4に記載の方法。
- 工程(b)に用いられるエネルギー線が紫外線光である、請求項4に記載の方法。
- 工程(b)の反応が30分〜30時間行われる、請求項4に記載の方法。
- 工程(b)の反応が溶媒の存在下で行われる、請求項4に記載の方法。
- 溶媒が酢酸エチル、アセトン、水、メタノール又はそれらの混合物である、請求項11に記載の方法。
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
TW093131887A TWI279403B (en) | 2004-10-20 | 2004-10-20 | Cyclobutanetetracarboxylate compound and preparation method thereof |
TW093131887 | 2004-10-20 |
Publications (2)
Publication Number | Publication Date |
---|---|
JP2006117673A true JP2006117673A (ja) | 2006-05-11 |
JP4977353B2 JP4977353B2 (ja) | 2012-07-18 |
Family
ID=36206993
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2005303996A Active JP4977353B2 (ja) | 2004-10-20 | 2005-10-19 | シクロブタンテトラカルボキシレート化合物及びその製造方法 |
Country Status (3)
Country | Link |
---|---|
US (2) | US20060089505A1 (ja) |
JP (1) | JP4977353B2 (ja) |
TW (1) | TWI279403B (ja) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2008273876A (ja) * | 2007-04-27 | 2008-11-13 | Nof Corp | 1,2,3,4−シクロブタンテトラカルボン酸の製造方法 |
JP2014522413A (ja) * | 2011-06-08 | 2014-09-04 | バイオジェン・アイデック・エムエイ・インコーポレイテッド | 高純度結晶性ジメチルフマラートの調製方法 |
WO2015108170A1 (ja) * | 2014-01-17 | 2015-07-23 | 日産化学工業株式会社 | シクロブタンテトラカルボン酸及びその無水物の製造方法 |
WO2015170713A1 (ja) * | 2014-05-09 | 2015-11-12 | 日産化学工業株式会社 | 1,3-ジ置換シクロブタン-1,2,3,4-テトラカルボン酸及び該酸二無水物の新規な製造方法 |
Families Citing this family (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP5639764B2 (ja) * | 2007-03-08 | 2014-12-10 | シンク−アールエックス,リミティド | 運動する器官と共に使用するイメージング及びツール |
MX2011001341A (es) | 2008-08-19 | 2011-03-29 | Xenoport Inc | Prodrogas de metil hidrogeno fumarato, sus composiciones farmaceuticas, y metodos de uso. |
CN102432464A (zh) * | 2011-12-14 | 2012-05-02 | 费近峰 | 一种富马酸二甲酯的连续生产工艺 |
AU2013305684B2 (en) | 2012-08-22 | 2016-11-24 | Xenoport, Inc. | Oral dosage forms of methyl hydrogen fumarate and prodrugs thereof |
US10945984B2 (en) | 2012-08-22 | 2021-03-16 | Arbor Pharmaceuticals, Llc | Methods of administering monomethyl fumarate and prodrugs thereof having reduced side effects |
WO2014160633A1 (en) | 2013-03-24 | 2014-10-02 | Xenoport, Inc. | Pharmaceutical compositions of dimethyl fumarate |
WO2014197860A1 (en) | 2013-06-07 | 2014-12-11 | Xenoport, Inc. | Method of making monomethyl fumarate |
WO2014205392A1 (en) | 2013-06-21 | 2014-12-24 | Xenoport, Inc. | Cocrystals of dimethyl fumarate |
JP2016534133A (ja) | 2013-09-06 | 2016-11-04 | ゼノポート,インコーポレイティド | (n,n−ジエチルカルバモイル)メチル メチル(2e)ブト−2−エン−1,4−ジオエートの結晶形態、その合成方法及び使用 |
JP6565686B2 (ja) * | 2014-01-17 | 2019-08-28 | 日産化学株式会社 | シクロブタンテトラカルボン酸誘導体の製造方法 |
US9999672B2 (en) | 2014-03-24 | 2018-06-19 | Xenoport, Inc. | Pharmaceutical compositions of fumaric acid esters |
CN104151165B (zh) * | 2014-08-11 | 2016-08-24 | 广东东阳光药业有限公司 | 制备富马酸二甲酯的方法 |
CN114516882A (zh) * | 2020-11-19 | 2022-05-20 | 烟台弘邦医药科技有限公司 | 一种环烷烃四羧酸二酐的制备方法 |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3139395A (en) * | 1961-01-09 | 1964-06-30 | American Cyanamid Co | Photodimerization of fumaric acid derivatives |
US3236801A (en) * | 1963-01-30 | 1966-02-22 | Exxon Research Engineering Co | Esters of 1, 2, 3, 4-cyclobutanetetracarboxylic acid and plastic compositions comprising same |
US3253016A (en) * | 1961-01-09 | 1966-05-24 | American Cyanamid Co | Thermal isomerization of the tetramethyl ester of cis, trans, cis-1, 2, 3, 4-cyclobutanetetracarboxylic acid |
CN1103398A (zh) * | 1993-11-30 | 1995-06-07 | 张治明 | 一种由顺酐生产富马酸二甲酯的工艺方法 |
-
2004
- 2004-10-20 TW TW093131887A patent/TWI279403B/zh active
-
2005
- 2005-10-19 US US11/253,798 patent/US20060089505A1/en not_active Abandoned
- 2005-10-19 JP JP2005303996A patent/JP4977353B2/ja active Active
-
2007
- 2007-08-02 US US11/888,703 patent/US7402693B2/en active Active
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3139395A (en) * | 1961-01-09 | 1964-06-30 | American Cyanamid Co | Photodimerization of fumaric acid derivatives |
US3253016A (en) * | 1961-01-09 | 1966-05-24 | American Cyanamid Co | Thermal isomerization of the tetramethyl ester of cis, trans, cis-1, 2, 3, 4-cyclobutanetetracarboxylic acid |
US3236801A (en) * | 1963-01-30 | 1966-02-22 | Exxon Research Engineering Co | Esters of 1, 2, 3, 4-cyclobutanetetracarboxylic acid and plastic compositions comprising same |
CN1103398A (zh) * | 1993-11-30 | 1995-06-07 | 张治明 | 一种由顺酐生产富马酸二甲酯的工艺方法 |
Cited By (16)
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JP2008273876A (ja) * | 2007-04-27 | 2008-11-13 | Nof Corp | 1,2,3,4−シクロブタンテトラカルボン酸の製造方法 |
JP2014522413A (ja) * | 2011-06-08 | 2014-09-04 | バイオジェン・アイデック・エムエイ・インコーポレイテッド | 高純度結晶性ジメチルフマラートの調製方法 |
JP6385273B6 (ja) | 2011-06-08 | 2023-12-15 | バイオジェン・エムエイ・インコーポレイテッド | 高純度結晶性ジメチルフマラートの調製方法 |
JP2020079247A (ja) * | 2014-01-17 | 2020-05-28 | 日産化学株式会社 | シクロブタンテトラカルボン酸及びその無水物の製造方法 |
KR20160108334A (ko) * | 2014-01-17 | 2016-09-19 | 닛산 가가쿠 고교 가부시키 가이샤 | 시클로부탄테트라카르복실산 및 그 무수물의 제조 방법 |
JPWO2015108170A1 (ja) * | 2014-01-17 | 2017-03-23 | 日産化学工業株式会社 | シクロブタンテトラカルボン酸及びその無水物の製造方法 |
KR20210013332A (ko) * | 2014-01-17 | 2021-02-03 | 닛산 가가쿠 가부시키가이샤 | 시클로부탄테트라카르복실산 및 그 무수물의 제조 방법 |
KR102247402B1 (ko) | 2014-01-17 | 2021-04-30 | 닛산 가가쿠 가부시키가이샤 | 시클로부탄테트라카르복실산 및 그 무수물의 제조 방법 |
KR102272227B1 (ko) * | 2014-01-17 | 2021-07-01 | 닛산 가가쿠 가부시키가이샤 | 시클로부탄테트라카르복실산 및 그 무수물의 제조 방법 |
WO2015108170A1 (ja) * | 2014-01-17 | 2015-07-23 | 日産化学工業株式会社 | シクロブタンテトラカルボン酸及びその無水物の製造方法 |
KR20170003949A (ko) * | 2014-05-09 | 2017-01-10 | 닛산 가가쿠 고교 가부시키 가이샤 | 1,3-디치환 시클로부탄-1,2,3,4-테트라카르복실산 및 그 산 2 무수물의 신규의 제조 방법 |
CN106458825A (zh) * | 2014-05-09 | 2017-02-22 | 日产化学工业株式会社 | 1,3‑二取代环丁烷‑1,2,3,4‑四羧酸及其酸二酐的新型制造方法 |
WO2015170713A1 (ja) * | 2014-05-09 | 2015-11-12 | 日産化学工業株式会社 | 1,3-ジ置換シクロブタン-1,2,3,4-テトラカルボン酸及び該酸二無水物の新規な製造方法 |
JP2020090531A (ja) * | 2014-05-09 | 2020-06-11 | 日産化学株式会社 | 1,3−ジ置換シクロブタン−1,2,3,4−テトラカルボン酸及び該酸二無水物の新規な製造方法 |
KR102342657B1 (ko) * | 2014-05-09 | 2021-12-22 | 닛산 가가쿠 가부시키가이샤 | 1,3-디치환 시클로부탄-1,2,3,4-테트라카르복실산 및 그 산 2 무수물의 신규의 제조 방법 |
JP6996577B2 (ja) | 2014-05-09 | 2022-01-17 | 日産化学株式会社 | 1,3-ジ置換シクロブタン-1,2,3,4-テトラカルボン酸の新規な製造方法 |
Also Published As
Publication number | Publication date |
---|---|
JP4977353B2 (ja) | 2012-07-18 |
TWI279403B (en) | 2007-04-21 |
US20080033199A1 (en) | 2008-02-07 |
US20060089505A1 (en) | 2006-04-27 |
TW200613308A (en) | 2006-05-01 |
US7402693B2 (en) | 2008-07-22 |
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