JP2001518060A - トリシクロカルボン酸エステル、その製造法およびそれからなる香料 - Google Patents
トリシクロカルボン酸エステル、その製造法およびそれからなる香料Info
- Publication number
- JP2001518060A JP2001518060A JP52036497A JP52036497A JP2001518060A JP 2001518060 A JP2001518060 A JP 2001518060A JP 52036497 A JP52036497 A JP 52036497A JP 52036497 A JP52036497 A JP 52036497A JP 2001518060 A JP2001518060 A JP 2001518060A
- Authority
- JP
- Japan
- Prior art keywords
- formula
- acid ester
- carboxylic acid
- tricyclo
- reaction
- 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
- 239000003205 fragrance Substances 0.000 title claims description 12
- 238000004519 manufacturing process Methods 0.000 title abstract description 14
- 239000002253 acid Substances 0.000 title description 9
- 150000002148 esters Chemical class 0.000 title description 6
- 238000000034 method Methods 0.000 claims abstract description 17
- SAOSCTYRONNFTC-UHFFFAOYSA-N 2-methyl-decanoic acid Chemical compound CCCCCCCCC(C)C(O)=O SAOSCTYRONNFTC-UHFFFAOYSA-N 0.000 claims abstract description 13
- MYPACYPUAQYSLJ-UHFFFAOYSA-N 2-methyldec-8-enoic acid Chemical compound CC=CCCCCCC(C)C(O)=O MYPACYPUAQYSLJ-UHFFFAOYSA-N 0.000 claims abstract description 12
- 238000006243 chemical reaction Methods 0.000 claims description 37
- ZSWFCLXCOIISFI-UHFFFAOYSA-N cyclopentadiene Chemical compound C1C=CC=C1 ZSWFCLXCOIISFI-UHFFFAOYSA-N 0.000 claims description 36
- 125000004432 carbon atom Chemical group C* 0.000 claims description 16
- 125000000217 alkyl group Chemical group 0.000 claims description 15
- HECLRDQVFMWTQS-RGOKHQFPSA-N 1755-01-7 Chemical compound C1[C@H]2[C@@H]3CC=C[C@@H]3[C@@H]1C=C2 HECLRDQVFMWTQS-RGOKHQFPSA-N 0.000 claims description 10
- 238000002360 preparation method Methods 0.000 claims description 2
- 239000002304 perfume Substances 0.000 abstract description 3
- 150000001875 compounds Chemical class 0.000 description 15
- 150000001733 carboxylic acid esters Chemical class 0.000 description 14
- 239000002904 solvent Substances 0.000 description 14
- 239000003054 catalyst Substances 0.000 description 10
- PYRZPBDTPRQYKG-UHFFFAOYSA-N cyclopentene-1-carboxylic acid Chemical compound OC(=O)C1=CCCC1 PYRZPBDTPRQYKG-UHFFFAOYSA-N 0.000 description 10
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 9
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 8
- PHXHZIALCFFYRT-UHFFFAOYSA-N ethyl cyclopentene-1-carboxylate Chemical compound CCOC(=O)C1=CCCC1 PHXHZIALCFFYRT-UHFFFAOYSA-N 0.000 description 7
- 239000007858 starting material Substances 0.000 description 7
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 5
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 5
- 238000005698 Diels-Alder reaction Methods 0.000 description 4
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 4
- -1 ethyl deca-8-ene-2-carboxylate Chemical compound 0.000 description 4
- 239000011541 reaction mixture Substances 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 3
- 239000005973 Carvone Substances 0.000 description 3
- 239000002841 Lewis acid Substances 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
- 229910002091 carbon monoxide Inorganic materials 0.000 description 3
- 238000004817 gas chromatography Methods 0.000 description 3
- 150000007517 lewis acids Chemical class 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- SCYULBFZEHDVBN-UHFFFAOYSA-N 1,1-Dichloroethane Chemical compound CC(Cl)Cl SCYULBFZEHDVBN-UHFFFAOYSA-N 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- 239000003377 acid catalyst Substances 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 239000011203 carbon fibre reinforced carbon Substances 0.000 description 2
- 238000006473 carboxylation reaction Methods 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- LPIQUOYDBNQMRZ-UHFFFAOYSA-N cyclopentene Chemical compound C1CC=CC1 LPIQUOYDBNQMRZ-UHFFFAOYSA-N 0.000 description 2
- DIOQZVSQGTUSAI-UHFFFAOYSA-N decane Chemical compound CCCCCCCCCC DIOQZVSQGTUSAI-UHFFFAOYSA-N 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 238000007086 side reaction Methods 0.000 description 2
- 235000017557 sodium bicarbonate Nutrition 0.000 description 2
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- NWUYHJFMYQTDRP-UHFFFAOYSA-N 1,2-bis(ethenyl)benzene;1-ethenyl-2-ethylbenzene;styrene Chemical compound C=CC1=CC=CC=C1.CCC1=CC=CC=C1C=C.C=CC1=CC=CC=C1C=C NWUYHJFMYQTDRP-UHFFFAOYSA-N 0.000 description 1
- CYSGHNMQYZDMIA-UHFFFAOYSA-N 1,3-Dimethyl-2-imidazolidinon Chemical compound CN1CCN(C)C1=O CYSGHNMQYZDMIA-UHFFFAOYSA-N 0.000 description 1
- 238000005160 1H NMR spectroscopy Methods 0.000 description 1
- NIONDZDPPYHYKY-UHFFFAOYSA-N 2-hexenoic acid Chemical compound CCCC=CC(O)=O NIONDZDPPYHYKY-UHFFFAOYSA-N 0.000 description 1
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- BDAGIHXWWSANSR-UHFFFAOYSA-M Formate Chemical compound [O-]C=O BDAGIHXWWSANSR-UHFFFAOYSA-M 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- OWIKHYCFFJSOEH-UHFFFAOYSA-N Isocyanic acid Chemical compound N=C=O OWIKHYCFFJSOEH-UHFFFAOYSA-N 0.000 description 1
- 238000005684 Liebig rearrangement reaction Methods 0.000 description 1
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-N Propionic acid Chemical compound CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 1
- 239000007868 Raney catalyst Substances 0.000 description 1
- 229910000564 Raney nickel Inorganic materials 0.000 description 1
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical class [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- XLJMAIOERFSOGZ-UHFFFAOYSA-N anhydrous cyanic acid Natural products OC#N XLJMAIOERFSOGZ-UHFFFAOYSA-N 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000012267 brine Substances 0.000 description 1
- 229910002090 carbon oxide Inorganic materials 0.000 description 1
- 150000007942 carboxylates Chemical class 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 238000010531 catalytic reduction reaction Methods 0.000 description 1
- 239000003729 cation exchange resin Substances 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 238000004440 column chromatography Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- HANKSFAYJLDDKP-UHFFFAOYSA-N dihydrodicyclopentadiene Chemical compound C12CC=CC2C2CCC1C2 HANKSFAYJLDDKP-UHFFFAOYSA-N 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- KGKUZGKMSKOEOK-UHFFFAOYSA-N ethyl 2-methyldecanoate Chemical compound CCCCCCCCC(C)C(=O)OCC KGKUZGKMSKOEOK-UHFFFAOYSA-N 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- 239000012454 non-polar solvent Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- RGSFGYAAUTVSQA-UHFFFAOYSA-N pentamethylene Natural products C1CCCC1 RGSFGYAAUTVSQA-UHFFFAOYSA-N 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 238000006722 reduction reaction Methods 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 1
- 239000011973 solid acid Substances 0.000 description 1
- 230000001629 suppression Effects 0.000 description 1
- 230000002194 synthesizing effect Effects 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 238000005979 thermal decomposition reaction Methods 0.000 description 1
- 239000002341 toxic gas Substances 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11B—PRODUCING, e.g. BY PRESSING RAW MATERIALS OR BY EXTRACTION FROM WASTE MATERIALS, REFINING OR PRESERVING FATS, FATTY SUBSTANCES, e.g. LANOLIN, FATTY OILS OR WAXES; ESSENTIAL OILS; PERFUMES
- C11B9/00—Essential oils; Perfumes
- C11B9/0042—Essential oils; Perfumes compounds containing condensed hydrocarbon rings
-
- 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
- C07C69/753—Esters of carboxylic acids having an esterified carboxyl group bound to a carbon atom of a ring other than a six-membered aromatic ring of polycyclic acids
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2603/00—Systems containing at least three condensed rings
- C07C2603/56—Ring systems containing bridged rings
- C07C2603/58—Ring systems containing bridged rings containing three rings
- C07C2603/60—Ring systems containing bridged rings containing three rings containing at least one ring with less than six members
- C07C2603/66—Ring systems containing bridged rings containing three rings containing at least one ring with less than six members containing five-membered rings
- C07C2603/68—Dicyclopentadienes; Hydrogenated dicyclopentadienes
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Fats And Perfumes (AREA)
Abstract
Description
Claims (1)
- 【特許請求の範囲】 1.式(I): (式中、Rは、1〜3個の炭素原子を有するアルキル基を示す) で表わされるトリシクロ〔5.2.1.02.6〕デカ−8−エン−2−カルボン 酸エステル。 2.式(II): (式中、Rは、1〜3個の炭素原子を有するアルキル基を示す) で表わされるシクロペンテニルカルボン酸エステルと、シクロペンタジエンとを 反応させる工程を有する、式(I): (式中、Rは、前記と同じ) で表わされるトリシクロ〔5.2.1.02.6〕デカ−8−エン−2−カルボン 酸エステルの製造法。 3. 反応溶液中でジシクロペンタジエンの熱分解により、シクロペンタジエン を製造する請求項2記載の製造法。 4.式(I):(式中、Rは、1〜3個の炭素原子を有するアルキル基を示す) で表わされるトリシクロ〔5.2.1.02.6〕デカ−8−エン−2−カルボン 酸エステルの二重結合を還元する工程を有する、式(III): (式中、Rは、前記と同じ) で表わされるトリシクロ〔5.2.1.02.6〕デカン−2−カルボン酸エステ ルの製造法。 5.式(I): (式中、Rは、1〜3個の炭素原子を有するアルキル基を示す) で表わされるトリシクロ〔5.2.1.02.6〕デカン−2−カルボン酸エステ ルからなる香料。
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP7-338287 | 1995-11-30 | ||
JP7338287A JP2802486B2 (ja) | 1995-11-30 | 1995-11-30 | トリシクロカルボン酸エステルおよびその製造法 |
PCT/JP1996/003483 WO1997019906A1 (en) | 1995-11-30 | 1996-11-27 | Tricyclocarboxylate, method for preparing the same and perfume comprising the same |
Publications (2)
Publication Number | Publication Date |
---|---|
JP2001518060A true JP2001518060A (ja) | 2001-10-09 |
JP3828154B2 JP3828154B2 (ja) | 2006-10-04 |
Family
ID=18316715
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP7338287A Expired - Lifetime JP2802486B2 (ja) | 1995-11-30 | 1995-11-30 | トリシクロカルボン酸エステルおよびその製造法 |
JP52036497A Expired - Fee Related JP3828154B2 (ja) | 1995-11-30 | 1996-11-27 | トリシクロカルボン酸エステル、その製造法およびそれからなる香料 |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP7338287A Expired - Lifetime JP2802486B2 (ja) | 1995-11-30 | 1995-11-30 | トリシクロカルボン酸エステルおよびその製造法 |
Country Status (7)
Country | Link |
---|---|
US (1) | US5811610A (ja) |
EP (1) | EP0807100B1 (ja) |
JP (2) | JP2802486B2 (ja) |
CN (2) | CN1142903C (ja) |
DE (1) | DE69606389T2 (ja) |
ES (1) | ES2143792T3 (ja) |
WO (1) | WO1997019906A1 (ja) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR100744823B1 (ko) * | 2006-02-15 | 2007-08-01 | 한국과학기술연구원 | (2-시클로펜테닐)클로로실란 유도체와 이의 제조방법 |
RU2582339C2 (ru) | 2010-05-27 | 2016-04-27 | Таргасепт, Инк. | Неконкурентные антагонисты никотиновых рецепторов |
WO2019159906A1 (ja) * | 2018-02-16 | 2019-08-22 | 三菱瓦斯化学株式会社 | トリシクロ[5.2.1.02,6]デカン-2-カルボン酸エステルの製造方法 |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS56128735A (en) * | 1980-03-14 | 1981-10-08 | Kao Corp | Ester of tricyclic carboxylic acid having perfume |
US4411828A (en) * | 1980-03-14 | 1983-10-25 | Kao Corporation | Fragrant tricyclic carboxylates |
JP2680069B2 (ja) * | 1988-10-07 | 1997-11-19 | 三菱瓦斯化学株式会社 | トリシクロデカンカルボン酸エステルの製造法 |
-
1995
- 1995-11-30 JP JP7338287A patent/JP2802486B2/ja not_active Expired - Lifetime
-
1996
- 1996-11-27 JP JP52036497A patent/JP3828154B2/ja not_active Expired - Fee Related
- 1996-11-27 WO PCT/JP1996/003483 patent/WO1997019906A1/en active IP Right Grant
- 1996-11-27 CN CNB001328271A patent/CN1142903C/zh not_active Expired - Lifetime
- 1996-11-27 CN CN96191672A patent/CN1071737C/zh not_active Expired - Lifetime
- 1996-11-27 ES ES96940141T patent/ES2143792T3/es not_active Expired - Lifetime
- 1996-11-27 EP EP96940141A patent/EP0807100B1/en not_active Expired - Lifetime
- 1996-11-27 US US08/875,396 patent/US5811610A/en not_active Expired - Lifetime
- 1996-11-27 DE DE69606389T patent/DE69606389T2/de not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
JP3828154B2 (ja) | 2006-10-04 |
JPH09151164A (ja) | 1997-06-10 |
EP0807100B1 (en) | 2000-01-26 |
US5811610A (en) | 1998-09-22 |
CN1308053A (zh) | 2001-08-15 |
CN1142903C (zh) | 2004-03-24 |
EP0807100A1 (en) | 1997-11-19 |
CN1071737C (zh) | 2001-09-26 |
DE69606389T2 (de) | 2000-05-25 |
CN1169712A (zh) | 1998-01-07 |
ES2143792T3 (es) | 2000-05-16 |
JP2802486B2 (ja) | 1998-09-24 |
WO1997019906A1 (en) | 1997-06-05 |
DE69606389D1 (de) | 2000-03-02 |
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