JPS5965035A - トランス−イソオイゲノ−ルおよびその誘導体の製法 - Google Patents
トランス−イソオイゲノ−ルおよびその誘導体の製法Info
- Publication number
- JPS5965035A JPS5965035A JP57173967A JP17396782A JPS5965035A JP S5965035 A JPS5965035 A JP S5965035A JP 57173967 A JP57173967 A JP 57173967A JP 17396782 A JP17396782 A JP 17396782A JP S5965035 A JPS5965035 A JP S5965035A
- Authority
- JP
- Japan
- Prior art keywords
- eugenol
- reaction
- formula
- catalyst
- 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.)
- Granted
Links
- BJIOGJUNALELMI-ONEGZZNKSA-N trans-isoeugenol Chemical compound COC1=CC(\C=C\C)=CC=C1O BJIOGJUNALELMI-ONEGZZNKSA-N 0.000 title description 10
- BJIOGJUNALELMI-UHFFFAOYSA-N trans-isoeugenol Natural products COC1=CC(C=CC)=CC=C1O BJIOGJUNALELMI-UHFFFAOYSA-N 0.000 title description 8
- 238000002360 preparation method Methods 0.000 title description 2
- RRAFCDWBNXTKKO-UHFFFAOYSA-N eugenol Chemical compound COC1=CC(CC=C)=CC=C1O RRAFCDWBNXTKKO-UHFFFAOYSA-N 0.000 claims abstract description 42
- NPBVQXIMTZKSBA-UHFFFAOYSA-N Chavibetol Natural products COC1=CC=C(CC=C)C=C1O NPBVQXIMTZKSBA-UHFFFAOYSA-N 0.000 claims abstract description 21
- 239000005770 Eugenol Substances 0.000 claims abstract description 21
- UVMRYBDEERADNV-UHFFFAOYSA-N Pseudoeugenol Natural products COC1=CC(C(C)=C)=CC=C1O UVMRYBDEERADNV-UHFFFAOYSA-N 0.000 claims abstract description 21
- 229960002217 eugenol Drugs 0.000 claims abstract description 21
- 238000006317 isomerization reaction Methods 0.000 claims abstract description 20
- 239000003054 catalyst Substances 0.000 claims abstract description 17
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 14
- 125000002252 acyl group Chemical group 0.000 claims abstract description 3
- 125000003710 aryl alkyl group Chemical group 0.000 claims abstract description 3
- 238000004519 manufacturing process Methods 0.000 claims description 8
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 2
- 238000006243 chemical reaction Methods 0.000 abstract description 22
- 150000001875 compounds Chemical class 0.000 abstract description 5
- 229910021639 Iridium tetrachloride Inorganic materials 0.000 abstract description 3
- 239000003205 fragrance Substances 0.000 abstract description 2
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 150000004682 monohydrates Chemical class 0.000 abstract 1
- LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 abstract 1
- CALMYRPSSNRCFD-UHFFFAOYSA-J tetrachloroiridium Chemical compound Cl[Ir](Cl)(Cl)Cl CALMYRPSSNRCFD-UHFFFAOYSA-J 0.000 abstract 1
- 239000000047 product Substances 0.000 description 12
- 238000000034 method Methods 0.000 description 7
- -1 PdC1 Chemical class 0.000 description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- SCCDQYPEOIRVGX-UHFFFAOYSA-N Acetyleugenol Chemical compound COC1=CC(CC=C)=CC=C1OC(C)=O SCCDQYPEOIRVGX-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- 230000035484 reaction time Effects 0.000 description 3
- DYLIWHYUXAJDOJ-OWOJBTEDSA-N (e)-4-(6-aminopurin-9-yl)but-2-en-1-ol Chemical compound NC1=NC=NC2=C1N=CN2C\C=C\CO DYLIWHYUXAJDOJ-OWOJBTEDSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 2
- 102000001708 Protein Isoforms Human genes 0.000 description 2
- 108010029485 Protein Isoforms Proteins 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- ZSIAUFGUXNUGDI-UHFFFAOYSA-N hexan-1-ol Chemical compound CCCCCCO ZSIAUFGUXNUGDI-UHFFFAOYSA-N 0.000 description 2
- KDLHZDBZIXYQEI-UHFFFAOYSA-N palladium Substances [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 2
- 150000002940 palladium Chemical class 0.000 description 2
- 230000000737 periodic effect Effects 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- MNXDNTVRAJQSAP-UHFFFAOYSA-N 1-hexoxy-2-methoxy-4-prop-2-enylbenzene Chemical compound CCCCCCOC1=CC=C(CC=C)C=C1OC MNXDNTVRAJQSAP-UHFFFAOYSA-N 0.000 description 1
- FDHXEIOBIOVBEN-UHFFFAOYSA-N 2-hydroxy-3-methoxy-5-prop-2-enylbenzaldehyde Chemical compound COC1=CC(CC=C)=CC(C=O)=C1O FDHXEIOBIOVBEN-UHFFFAOYSA-N 0.000 description 1
- JEQOQDNQQSEKIA-UHFFFAOYSA-N 2-methoxy-1-pentoxy-4-prop-2-enylbenzene Chemical compound CCCCCOC1=CC=C(CC=C)C=C1OC JEQOQDNQQSEKIA-UHFFFAOYSA-N 0.000 description 1
- ORCYFVZXLWZLMC-UHFFFAOYSA-N 2-methoxy-4-prop-2-enyl-1-propoxybenzene Chemical compound CCCOC1=CC=C(CC=C)C=C1OC ORCYFVZXLWZLMC-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- XTHFKEDIFFGKHM-UHFFFAOYSA-N Dimethoxyethane Chemical compound COCCOC XTHFKEDIFFGKHM-UHFFFAOYSA-N 0.000 description 1
- 101100028920 Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) cfp gene Proteins 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- ZYEMGPIYFIJGTP-UHFFFAOYSA-N O-methyleugenol Chemical compound COC1=CC=C(CC=C)C=C1OC ZYEMGPIYFIJGTP-UHFFFAOYSA-N 0.000 description 1
- 240000007594 Oryza sativa Species 0.000 description 1
- 235000007164 Oryza sativa Nutrition 0.000 description 1
- ZVQOOHYFBIDMTQ-UHFFFAOYSA-N [methyl(oxido){1-[6-(trifluoromethyl)pyridin-3-yl]ethyl}-lambda(6)-sulfanylidene]cyanamide Chemical compound N#CN=S(C)(=O)C(C)C1=CC=C(C(F)(F)F)N=C1 ZVQOOHYFBIDMTQ-UHFFFAOYSA-N 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 239000003518 caustics Substances 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000004020 conductor Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 230000008878 coupling Effects 0.000 description 1
- 238000010168 coupling process Methods 0.000 description 1
- 238000005859 coupling reaction Methods 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- NBVXSUQYWXRMNV-UHFFFAOYSA-N fluoromethane Chemical compound FC NBVXSUQYWXRMNV-UHFFFAOYSA-N 0.000 description 1
- 159000000011 group IA salts Chemical class 0.000 description 1
- 239000000852 hydrogen donor Substances 0.000 description 1
- 239000003701 inert diluent Substances 0.000 description 1
- 239000010410 layer Substances 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000007670 refining Methods 0.000 description 1
- 235000009566 rice Nutrition 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/52—Improvements relating to the production of bulk chemicals using catalysts, e.g. selective catalysts
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Catalysts (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP57173967A JPS5965035A (ja) | 1982-10-05 | 1982-10-05 | トランス−イソオイゲノ−ルおよびその誘導体の製法 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP57173967A JPS5965035A (ja) | 1982-10-05 | 1982-10-05 | トランス−イソオイゲノ−ルおよびその誘導体の製法 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5965035A true JPS5965035A (ja) | 1984-04-13 |
| JPS64374B2 JPS64374B2 (enrdf_load_html_response) | 1989-01-06 |
Family
ID=15970349
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP57173967A Granted JPS5965035A (ja) | 1982-10-05 | 1982-10-05 | トランス−イソオイゲノ−ルおよびその誘導体の製法 |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5965035A (enrdf_load_html_response) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN107188788A (zh) * | 2017-05-26 | 2017-09-22 | 浙江大学 | 一种丁香酚纯化方法 |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5123229A (enrdf_load_html_response) * | 1974-07-31 | 1976-02-24 | Kobayashi Perfumery Co |
-
1982
- 1982-10-05 JP JP57173967A patent/JPS5965035A/ja active Granted
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5123229A (enrdf_load_html_response) * | 1974-07-31 | 1976-02-24 | Kobayashi Perfumery Co |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN107188788A (zh) * | 2017-05-26 | 2017-09-22 | 浙江大学 | 一种丁香酚纯化方法 |
| CN107188788B (zh) * | 2017-05-26 | 2020-05-29 | 浙江大学 | 一种丁香酚纯化方法 |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS64374B2 (enrdf_load_html_response) | 1989-01-06 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| Moss et al. | Photolysis of phenyldiazomethane in olefinic matrices. Chemistry of triplet phenylcarbene | |
| Corre et al. | Regioselective hydrosilylation of terminal alkynes using pentamethylcyclopentadienyl iridium (III) metallacycle catalysts | |
| Marino et al. | Chemistry of substituted (. alpha.-carbethoxyvinyl) cuprates. 2. Stereospecific olefin synthesis | |
| CN107417505A (zh) | α‑卤代四甲基环己酮及其与（2,3,4,4‑四甲基环戊基）甲基羧酸酯的制备方法 | |
| JPS6215536B2 (enrdf_load_html_response) | ||
| NO122978B (enrdf_load_html_response) | ||
| US4460786A (en) | Process for the selective addition of a compound having an activated carbon atom onto a substituted conjugated diene | |
| JPS59212446A (ja) | ４−ペンテン酸エステルの製法 | |
| US4028385A (en) | Process for preparing stereospecific farnesylacetic acid and ester thereof | |
| US5068214A (en) | Process for the preparation of a catalyst | |
| JPS5965035A (ja) | トランス−イソオイゲノ−ルおよびその誘導体の製法 | |
| US4393245A (en) | Musk-like scents and their manufacture | |
| Westberg et al. | Thermolysis of pentacyclo [4.4. 0.0. 2, 50.3, 804, 7] dec-9-ene | |
| US3996290A (en) | 2,4-Dimethyl-2-phenyl-4-pentenal | |
| Braude et al. | 461. Alkenylation employing lithium alkenyls. Part V. The formation and some reactions of cis-propenyl-lithium | |
| US4029709A (en) | Process for the hydrogenation of citral to citronellal and of citronellal to citronellol using chromium-promoted Raney nickel catalyst | |
| Hart et al. | Bridged ionic intermediates in the acylation of cyclopropanes | |
| Dobashi et al. | Kinetic investigation of the configurational isomerization of geometrically isomeric nitrones | |
| Coquerel et al. | Catalytic properties of the Pd/C-triethylamine system | |
| Gravel et al. | Synthesis and photochemistry of 4, 4-diphenyl-γ-pyran. Di-π-methane rearrangement in a new chromophore | |
| US4181683A (en) | 1,7-Octadien-3-one and process for preparing the same | |
| US4533751A (en) | Preparation of 1,3-dienamines from myrcene and substituted myrcene | |
| Beckwith et al. | E2 reactions of menthyl and neoisomenthyl Toluene-p-sulphonates | |
| Haaima et al. | Photoisomerisation of (E)-iodoalkylidene lactones a route to (Z)-iodoalkylidene Lactones | |
| EP0110142B1 (fr) | Procédé pour la préparation de cyclopenténones alkylées et esters acétyléniques utiles en tant que produits de départ dans ladite préparation |