GB1076306A - A process for the manufacture of isocryptoxanthin and echinenone - Google Patents
A process for the manufacture of isocryptoxanthin and echinenoneInfo
- Publication number
- GB1076306A GB1076306A GB17635/66A GB1763566A GB1076306A GB 1076306 A GB1076306 A GB 1076306A GB 17635/66 A GB17635/66 A GB 17635/66A GB 1763566 A GB1763566 A GB 1763566A GB 1076306 A GB1076306 A GB 1076306A
- Authority
- GB
- United Kingdom
- Prior art keywords
- echinenone
- isocryptoxanthin
- retinene
- isomerized
- trans
- 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
Links
- QXNWZXMBUKUYMD-ITUXNECMSA-N 4-keto-beta-carotene Chemical compound CC=1C(=O)CCC(C)(C)C=1/C=C/C(/C)=C/C=C/C(/C)=C/C=C/C=C(C)C=CC=C(C)C=CC1=C(C)CCCC1(C)C QXNWZXMBUKUYMD-ITUXNECMSA-N 0.000 title abstract 4
- JCRCKXUPYKELBT-QQGJMDNJSA-N 4-hydroxy-all-trans-beta-carotene Chemical compound CC=1C(O)CCC(C)(C)C=1\C=C\C(\C)=C\C=C\C(\C)=C\C=C\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C JCRCKXUPYKELBT-QQGJMDNJSA-N 0.000 title abstract 3
- JCRCKXUPYKELBT-ITUXNECMSA-N all-trans isocryptoxanthin Natural products CC(=C/C=C/C=C(C)/C=C/C=C(C)/C=C/C1=C(C)C(O)CCC1(C)C)C=CC=C(/C)C=CC2=C(C)CCCC2(C)C JCRCKXUPYKELBT-ITUXNECMSA-N 0.000 title abstract 3
- YXPMCBGFLULSGQ-YHEDCBSUSA-N echinenone Natural products CC(=C/C=C/C=C(C)/C=C/C=C(C)/C=C/C1=C(C)CCC(=O)C1(C)C)C=CC=C(/C)C=CC2=C(C)CCCC2(C)C YXPMCBGFLULSGQ-YHEDCBSUSA-N 0.000 title abstract 2
- 235000006932 echinenone Nutrition 0.000 title abstract 2
- 238000004519 manufacturing process Methods 0.000 title 1
- 238000000034 method Methods 0.000 title 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 abstract 3
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 abstract 2
- PCLIMKBDDGJMGD-UHFFFAOYSA-N N-bromosuccinimide Chemical compound BrN1C(=O)CCC1=O PCLIMKBDDGJMGD-UHFFFAOYSA-N 0.000 abstract 2
- 235000020945 retinal Nutrition 0.000 abstract 2
- 239000011604 retinal Substances 0.000 abstract 2
- 239000004215 Carbon black (E152) Substances 0.000 abstract 1
- NCYCYZXNIZJOKI-OVSJKPMPSA-N Retinaldehyde Chemical compound O=C\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C NCYCYZXNIZJOKI-OVSJKPMPSA-N 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- 125000004423 acyloxy group Chemical group 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 239000004411 aluminium Substances 0.000 abstract 1
- 229910052782 aluminium Inorganic materials 0.000 abstract 1
- -1 aluminium alkoxide Chemical class 0.000 abstract 1
- 150000001450 anions Chemical class 0.000 abstract 1
- 125000003710 aryl alkyl group Chemical group 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- QXNWZXMBUKUYMD-QQGJMDNJSA-N echinenone Chemical compound CC=1C(=O)CCC(C)(C)C=1\C=C\C(\C)=C\C=C\C(\C)=C\C=C\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C QXNWZXMBUKUYMD-QQGJMDNJSA-N 0.000 abstract 1
- 238000010438 heat treatment Methods 0.000 abstract 1
- 229930195733 hydrocarbon Natural products 0.000 abstract 1
- 150000002430 hydrocarbons Chemical class 0.000 abstract 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 1
- 239000001257 hydrogen Substances 0.000 abstract 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 1
- 229910052500 inorganic mineral Inorganic materials 0.000 abstract 1
- 239000011707 mineral Substances 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 230000003647 oxidation Effects 0.000 abstract 1
- 238000007254 oxidation reaction Methods 0.000 abstract 1
- 238000002360 preparation method Methods 0.000 abstract 1
- 239000002904 solvent Substances 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C403/00—Derivatives of cyclohexane or of a cyclohexene or of cyclohexadiene, having a side-chain containing an acyclic unsaturated part of at least four carbon atoms, this part being directly attached to the cyclohexane or cyclohexene or cyclohexadiene rings, e.g. vitamin A, beta-carotene, beta-ionone
- C07C403/24—Derivatives of cyclohexane or of a cyclohexene or of cyclohexadiene, having a side-chain containing an acyclic unsaturated part of at least four carbon atoms, this part being directly attached to the cyclohexane or cyclohexene or cyclohexadiene rings, e.g. vitamin A, beta-carotene, beta-ionone having side-chains substituted by six-membered non-aromatic rings, e.g. beta-carotene
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C403/00—Derivatives of cyclohexane or of a cyclohexene or of cyclohexadiene, having a side-chain containing an acyclic unsaturated part of at least four carbon atoms, this part being directly attached to the cyclohexane or cyclohexene or cyclohexadiene rings, e.g. vitamin A, beta-carotene, beta-ionone
- C07C403/14—Derivatives of cyclohexane or of a cyclohexene or of cyclohexadiene, having a side-chain containing an acyclic unsaturated part of at least four carbon atoms, this part being directly attached to the cyclohexane or cyclohexene or cyclohexadiene rings, e.g. vitamin A, beta-carotene, beta-ionone having side-chains substituted by doubly-bound oxygen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/12—Systems containing only non-condensed rings with a six-membered ring
- C07C2601/16—Systems containing only non-condensed rings with a six-membered ring the ring being unsaturated
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US45163065A | 1965-04-28 | 1965-04-28 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1076306A true GB1076306A (en) | 1967-07-19 |
Family
ID=23793020
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB17635/66A Expired GB1076306A (en) | 1965-04-28 | 1966-04-22 | A process for the manufacture of isocryptoxanthin and echinenone |
Country Status (4)
| Country | Link |
|---|---|
| BE (1) | BE680076A (enrdf_load_html_response) |
| ES (1) | ES326062A1 (enrdf_load_html_response) |
| GB (1) | GB1076306A (enrdf_load_html_response) |
| NL (1) | NL6605422A (enrdf_load_html_response) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2008122988A1 (en) * | 2007-04-05 | 2008-10-16 | Cadila Healthcare Limited | Process for preparation of atovaquone and the conversion of cis-isomer to trans- isomer |
| CN113817299A (zh) * | 2021-08-18 | 2021-12-21 | 安徽建筑大学 | 一种具有离子和化学双重交联结构的pla基共混复合材料及其制备方法 |
-
1966
- 1966-04-22 NL NL6605422A patent/NL6605422A/xx unknown
- 1966-04-22 GB GB17635/66A patent/GB1076306A/en not_active Expired
- 1966-04-26 BE BE680076D patent/BE680076A/xx unknown
- 1966-04-27 ES ES0326062A patent/ES326062A1/es not_active Expired
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2008122988A1 (en) * | 2007-04-05 | 2008-10-16 | Cadila Healthcare Limited | Process for preparation of atovaquone and the conversion of cis-isomer to trans- isomer |
| CN113817299A (zh) * | 2021-08-18 | 2021-12-21 | 安徽建筑大学 | 一种具有离子和化学双重交联结构的pla基共混复合材料及其制备方法 |
| CN113817299B (zh) * | 2021-08-18 | 2022-12-13 | 安徽建筑大学 | 一种具有离子和化学双重交联结构的pla基共混复合材料及其制备方法 |
Also Published As
| Publication number | Publication date |
|---|---|
| ES326062A1 (es) | 1967-03-01 |
| BE680076A (enrdf_load_html_response) | 1966-10-26 |
| NL6605422A (enrdf_load_html_response) | 1966-10-31 |
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