EP0115278B1 - Verwendung der 1-Cyclopentenylessigsäure als Riechstoff, diesen enthaltende Duftzusammensetzung und parfumierte Produkte - Google Patents
Verwendung der 1-Cyclopentenylessigsäure als Riechstoff, diesen enthaltende Duftzusammensetzung und parfumierte Produkte Download PDFInfo
- Publication number
- EP0115278B1 EP0115278B1 EP84100217A EP84100217A EP0115278B1 EP 0115278 B1 EP0115278 B1 EP 0115278B1 EP 84100217 A EP84100217 A EP 84100217A EP 84100217 A EP84100217 A EP 84100217A EP 0115278 B1 EP0115278 B1 EP 0115278B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- perfuming
- acid
- cyclopentenylacetic
- composition containing
- ingredient
- 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
- 239000000203 mixture Substances 0.000 title claims description 13
- 239000004615 ingredient Substances 0.000 title claims description 8
- 239000012437 perfumed product Substances 0.000 title claims description 3
- 239000002453 shampoo Substances 0.000 claims description 4
- 239000000344 soap Substances 0.000 claims description 4
- 230000003796 beauty Effects 0.000 claims description 2
- 239000002537 cosmetic Substances 0.000 claims description 2
- 239000006071 cream Substances 0.000 claims description 2
- 239000003599 detergent Substances 0.000 claims description 2
- 239000004480 active ingredient Substances 0.000 claims 2
- -1 household articles Substances 0.000 claims 2
- 239000000454 talc Substances 0.000 claims 1
- 229910052623 talc Inorganic materials 0.000 claims 1
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- 239000002304 perfume Substances 0.000 description 6
- 239000002253 acid Substances 0.000 description 5
- 150000001875 compounds Chemical class 0.000 description 4
- FLKPEMZONWLCSK-UHFFFAOYSA-N diethyl phthalate Chemical compound CCOC(=O)C1=CC=CC=C1C(=O)OCC FLKPEMZONWLCSK-UHFFFAOYSA-N 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 235000012907 honey Nutrition 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000012074 organic phase Substances 0.000 description 2
- WLJVXDMOQOGPHL-UHFFFAOYSA-N phenylacetic acid Chemical compound OC(=O)CC1=CC=CC=C1 WLJVXDMOQOGPHL-UHFFFAOYSA-N 0.000 description 2
- QOGMZIQMZUXOKM-UHFFFAOYSA-N 2-(cyclopenten-1-yl)acetic acid Chemical compound OC(=O)CC1=CCCC1 QOGMZIQMZUXOKM-UHFFFAOYSA-N 0.000 description 1
- WLJVXDMOQOGPHL-PPJXEINESA-N 2-phenylacetic acid Chemical compound O[14C](=O)CC1=CC=CC=C1 WLJVXDMOQOGPHL-PPJXEINESA-N 0.000 description 1
- 239000008346 aqueous phase Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 150000005829 chemical entities Chemical class 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 235000009508 confectionery Nutrition 0.000 description 1
- KQENDZXFFPZPFV-UHFFFAOYSA-N cyclopentylidenemethyl acetate Chemical compound CC(=O)OC=C1CCCC1 KQENDZXFFPZPFV-UHFFFAOYSA-N 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 239000000796 flavoring agent Substances 0.000 description 1
- 235000019634 flavors Nutrition 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 150000004702 methyl esters Chemical class 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 230000020477 pH reduction Effects 0.000 description 1
- 229960003424 phenylacetic acid Drugs 0.000 description 1
- 239000003279 phenylacetic acid Substances 0.000 description 1
- 230000008092 positive effect Effects 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 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
- C11B9/0026—Essential oils; Perfumes compounds containing an alicyclic ring not condensed with another ring
- C11B9/003—Essential oils; Perfumes compounds containing an alicyclic ring not condensed with another ring the ring containing less than six carbon atoms
Definitions
- the present invention relates to the field of perfumery and more particularly it relates to the use of an unsaturated cycloaliphatic acid as a perfuming ingredient for the preparation of perfumes and perfumed products.
- 1-cyclopentenylacetic acid of the formula could be used to impart or improve the honey-like fragrant note of perfumes and scented products without having the specific secondary characteristics of phenylacetic acid.
- the 1-cyclopentenylacetic acid of the invention finds a very wide use both in fine perfumery and in technical applications, for example in the perfume of soaps, detergents, powder or liquids, cleaning articles or cosmetics, shampoos or beauty creams.
- the proportions in which the compound of the invention is used to develop the desired odorous effects can vary within a fairly wide range of values. Its power is such that quantities of the order of 1-10 r oo by weight relative to the weight of the composition or of the scented article may already be sufficient to obtain a positive effect. Concentrations of 0.1-2% are preferably used in the manufacture of concentrated compositions or "hearts".
- 1-cyclopentenylacetic acid can be added either directly to the product which one wishes to perfume, or, more often, in the form of a solution mixed with other perfuming ingredients.
- the co-ingredients, the solvents or the usual supports, the use of which is well known to those skilled in the art, are perfectly suitable for this purpose.
- the acid of the invention is a known chemical entity. Its preparation can be carried out according to the methods described [see for this purpose US Pat. No. 1,965,762] or from cyclopentylidene-methyl acetate [see US Pat. No. 4,280,934] by hydrolysis thereof according to the scheme that is here :
- reaction mixture was kept at 70 ° C overnight, then 2.5 l of water was added thereto and the methanol was evaporated. After acidification with HCl, separation of the organic phase, followed by re-extraction with ether of the aqueous phase, the two combined organic phases were distilled under reduced pressure.
- the desired product was obtained with a yield of 82.3% at Eb. 96 ° C / approx. 6.65 Pa. Traces of the isomeric compound of formula were also present in the product obtained, but their presence has no practical influence on the quantity of the main product.
- the 2-cyclopentenylacetic acid in solution at 25% in diethyl phthalate was added at a rate of 2% in a commercial soap paste with neutral odor and, according to the usual techniques, the resulting paste was used for the manufacture of bars of toilet soaps.
- the odor of the article thus obtained was judged by a group of experts who defined it as being characterized by a separate note of the “honey” type.
- a basic pink-type composition was prepared by mixing the following ingredients (parts by weight):
- a basic perfuming composition intended to be incorporated into a shampoo was prepared by mixing the following ingredients (parts by weight):
- the olfactory stability was also confirmed by tests of prolonged ultraviolet irradiation of the products obtained.
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Detergent Compositions (AREA)
- Fats And Perfumes (AREA)
- Cosmetics (AREA)
Claims (3)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH419/83 | 1983-01-26 | ||
CH41983 | 1983-01-26 |
Publications (3)
Publication Number | Publication Date |
---|---|
EP0115278A2 EP0115278A2 (de) | 1984-08-08 |
EP0115278A3 EP0115278A3 (en) | 1986-03-19 |
EP0115278B1 true EP0115278B1 (de) | 1988-03-02 |
Family
ID=4186596
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP84100217A Expired EP0115278B1 (de) | 1983-01-26 | 1984-01-11 | Verwendung der 1-Cyclopentenylessigsäure als Riechstoff, diesen enthaltende Duftzusammensetzung und parfumierte Produkte |
Country Status (4)
Country | Link |
---|---|
US (1) | US4584127A (de) |
EP (1) | EP0115278B1 (de) |
JP (1) | JPS59144714A (de) |
DE (1) | DE3469562D1 (de) |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5164364A (en) * | 1986-09-30 | 1992-11-17 | Givaudan Corporation | Ethyl campholenates and dihydro derivatives thereof as flavorants and odorants |
ES2047188T3 (es) * | 1989-04-27 | 1994-02-16 | Firmenich & Cie | Procedimiento de perfumado. |
US6720295B2 (en) * | 2001-08-27 | 2004-04-13 | Firmenich Sa | Use of tertiary alcohols or esters as perfuming ingredients |
JP4486549B2 (ja) * | 2005-06-06 | 2010-06-23 | 三菱重工業株式会社 | ガスタービンの燃焼器 |
EP2474301B1 (de) * | 2011-12-14 | 2014-04-16 | Symrise AG | Riechstoffmischungen enthaltend Cyclopent-2-Enyl-Essigsäureethylester |
US10876067B2 (en) | 2016-02-15 | 2020-12-29 | Symrise Ag | Fragrant mixtures containing esters and ketones |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US1965792A (en) * | 1931-03-06 | 1934-07-10 | Cie De Bethune | Esters of unsubstituted and alphasubstituted cyclopentenylacetic acid and their production |
US4031132A (en) * | 1974-07-19 | 1977-06-21 | Givaudan Corporation | Isopropenyl cyclopentene carboxylic acids |
CH616077A5 (de) * | 1976-06-30 | 1980-03-14 | Firmenich & Cie |
-
1984
- 1984-01-11 DE DE8484100217T patent/DE3469562D1/de not_active Expired
- 1984-01-11 EP EP84100217A patent/EP0115278B1/de not_active Expired
- 1984-01-12 US US06/570,177 patent/US4584127A/en not_active Expired - Fee Related
- 1984-01-24 JP JP59009629A patent/JPS59144714A/ja active Granted
Also Published As
Publication number | Publication date |
---|---|
JPS59144714A (ja) | 1984-08-18 |
EP0115278A3 (en) | 1986-03-19 |
EP0115278A2 (de) | 1984-08-08 |
JPS6127368B2 (de) | 1986-06-25 |
US4584127A (en) | 1986-04-22 |
DE3469562D1 (en) | 1988-04-07 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EP0180885B1 (de) | Verwendung eines cycloaliphatischen Carbinols als Riechstoff | |
EP2566838B1 (de) | Verbindungen mit einer holzigen note | |
EP0115278B1 (de) | Verwendung der 1-Cyclopentenylessigsäure als Riechstoff, diesen enthaltende Duftzusammensetzung und parfumierte Produkte | |
EP2203417B1 (de) | Substituierte octan(en)nitrile, verfahren zu deren synthese und deren anwendungen in der duftstoffherstellung | |
EP0584477B1 (de) | Verwendung einer Cyclopentadecenone als Parfümszutat | |
EP0544110B1 (de) | Tertiäre cyclische Alkohole und ihre Anwendung als Riechstoffbestandteile | |
EP0004968B1 (de) | Norbornen(-an)Derivate, Verfahren zu ihrer Herstellung und ihre Verwendung als Riechstoffe | |
JP4903144B2 (ja) | シトロネラおよびフローラル香料成分 | |
EP0051546B1 (de) | Verfahren zur Herstellung parfümierender Zusammensetzungen und parfümierter Produkte und so erhaltene Zusammensetzungen und Produkte | |
JP6005159B2 (ja) | 付香アセタール | |
JP5897119B2 (ja) | アロマティックノートを有するペンタ/ヘキサメチル−3,4,5,8−テトラヒドロ−1(2h)−ナフタレノン誘導体 | |
EP1069176B1 (de) | Aliphatische Ester und Ihre Verwendung als Duftstoff | |
EP0838215B1 (de) | Verwendung von ungesättigten aliphatischen Estern in der Parfümerie | |
EP0045534B1 (de) | Verwendung von Phenyl-n-hexyl-keton, als Riechstoff, und dieses Keton enthaltende Riechstoffkompositionen | |
JP6479001B2 (ja) | ウッディな匂いを有する化合物 | |
JP4041238B2 (ja) | 香料中で、およびフレーバリング成分としての2,5,6−トリメチル−2−ヘプタノールの使用 | |
EP2904079B1 (de) | Geschmacks- und duftformulierung | |
JP4128223B2 (ja) | 香料における環式ケトンの使用 | |
JP6016922B2 (ja) | スミレ葉着香剤 | |
EP0052115B1 (de) | Bicyclische verbindungen und ihre verwendung als riechstoffe | |
EP0181475B1 (de) | Ungesättigtes aliphatisches Keton und seine Verwendung als Parfümierungsbestandteil | |
EP0056500A2 (de) | Ester der 2,2,-Dimethyl-Propionsäure, ihre Verwendung als Riechstoffe und eine sie enthaltende Zusammensetzung | |
EP0081699A1 (de) | Alicyclische Verbindungen, ihre Verwendung als Riech- oder Aromastoffe und Verfahren zu ihrer Herstellung | |
WO1992003402A1 (fr) | Compose cetonique polycyclique et son utilisation a titre d'ingredient parfumant | |
JPH01160936A (ja) | 新規な発香化合物 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PUAI | Public reference made under article 153(3) epc to a published international application that has entered the european phase |
Free format text: ORIGINAL CODE: 0009012 |
|
17P | Request for examination filed |
Effective date: 19840111 |
|
AK | Designated contracting states |
Designated state(s): CH DE FR GB LI NL |
|
PUAL | Search report despatched |
Free format text: ORIGINAL CODE: 0009013 |
|
AK | Designated contracting states |
Kind code of ref document: A3 Designated state(s): CH DE FR GB LI NL |
|
17Q | First examination report despatched |
Effective date: 19861201 |
|
ITF | It: translation for a ep patent filed | ||
GRAA | (expected) grant |
Free format text: ORIGINAL CODE: 0009210 |
|
AK | Designated contracting states |
Kind code of ref document: B1 Designated state(s): CH DE FR GB LI NL |
|
GBT | Gb: translation of ep patent filed (gb section 77(6)(a)/1977) | ||
REF | Corresponds to: |
Ref document number: 3469562 Country of ref document: DE Date of ref document: 19880407 |
|
PLBE | No opposition filed within time limit |
Free format text: ORIGINAL CODE: 0009261 |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: NL Payment date: 19890131 Year of fee payment: 9 |
|
26N | No opposition filed | ||
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: NL Effective date: 19910801 |
|
NLV4 | Nl: lapsed or anulled due to non-payment of the annual fee | ||
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: FR Payment date: 19931208 Year of fee payment: 11 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: CH Payment date: 19931209 Year of fee payment: 11 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: GB Payment date: 19931210 Year of fee payment: 11 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: DE Payment date: 19931217 Year of fee payment: 11 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: GB Effective date: 19950111 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: CH Effective date: 19950131 Ref country code: LI Effective date: 19950131 |
|
GBPC | Gb: european patent ceased through non-payment of renewal fee |
Effective date: 19950111 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: FR Effective date: 19950929 |
|
REG | Reference to a national code |
Ref country code: CH Ref legal event code: PL |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: DE Effective date: 19951003 |
|
REG | Reference to a national code |
Ref country code: FR Ref legal event code: ST |