JP2014526571A - フレグランス化合物および組成物 - Google Patents
フレグランス化合物および組成物 Download PDFInfo
- Publication number
- JP2014526571A JP2014526571A JP2014528979A JP2014528979A JP2014526571A JP 2014526571 A JP2014526571 A JP 2014526571A JP 2014528979 A JP2014528979 A JP 2014528979A JP 2014528979 A JP2014528979 A JP 2014528979A JP 2014526571 A JP2014526571 A JP 2014526571A
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- JP
- Japan
- Prior art keywords
- ethyl
- formula
- fragrance
- compound
- methyl
- 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
- 150000001875 compounds Chemical class 0.000 title claims abstract description 32
- 239000003205 fragrance Substances 0.000 title claims abstract description 22
- 239000000203 mixture Substances 0.000 title claims description 30
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract description 8
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims abstract description 7
- 238000000034 method Methods 0.000 claims description 6
- 239000002304 perfume Substances 0.000 claims description 6
- 239000000796 flavoring agent Substances 0.000 claims description 3
- 235000019634 flavors Nutrition 0.000 claims description 3
- 239000004615 ingredient Substances 0.000 claims description 3
- OKPKEJYSFLOJKZ-UHFFFAOYSA-N 4-(3,3-dimethylcyclopentylidene)butanal Chemical compound CC1(C)CCC(=CCCC=O)C1 OKPKEJYSFLOJKZ-UHFFFAOYSA-N 0.000 claims description 2
- IWHQKUHIQVQXMA-UHFFFAOYSA-N 4-(3-ethyl-3-methylcyclopentylidene)butanal Chemical compound CCC1(C)CCC(=CCCC=O)C1 IWHQKUHIQVQXMA-UHFFFAOYSA-N 0.000 claims description 2
- 230000003796 beauty Effects 0.000 claims 1
- 230000008786 sensory perception of smell Effects 0.000 claims 1
- 239000000047 product Substances 0.000 description 27
- CHCCBPDEADMNCI-UHFFFAOYSA-N 3-Methyl-2-cyclopenten-1-one Chemical compound CC1=CC(=O)CC1 CHCCBPDEADMNCI-UHFFFAOYSA-N 0.000 description 9
- -1 tree moss absolute Substances 0.000 description 7
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 6
- 239000007788 liquid Substances 0.000 description 6
- 239000003921 oil Substances 0.000 description 6
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- ASCYPCBZHXTNAM-UHFFFAOYSA-N 1-ethenyl-3,3-dimethylcyclopentan-1-ol Chemical compound CC1(C)CCC(O)(C=C)C1 ASCYPCBZHXTNAM-UHFFFAOYSA-N 0.000 description 4
- RQWVQZYEZIMEIX-UHFFFAOYSA-N 1-ethenyl-3-ethyl-3-methylcyclopentan-1-ol Chemical compound CCC1(C)CCC(O)(C=C)C1 RQWVQZYEZIMEIX-UHFFFAOYSA-N 0.000 description 4
- JSYAQLZSGHPSJD-UHFFFAOYSA-N 3,3-dimethylcyclopentan-1-one Chemical compound CC1(C)CCC(=O)C1 JSYAQLZSGHPSJD-UHFFFAOYSA-N 0.000 description 4
- IUZULRVGAITOOO-UHFFFAOYSA-N 3-ethyl-3-methylcyclopentan-1-one Chemical compound CCC1(C)CCC(=O)C1 IUZULRVGAITOOO-UHFFFAOYSA-N 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- GLZPCOQZEFWAFX-UHFFFAOYSA-N Geraniol Chemical compound CC(C)=CCCC(C)=CCO GLZPCOQZEFWAFX-UHFFFAOYSA-N 0.000 description 4
- FJKIXWOMBXYWOQ-UHFFFAOYSA-N ethenoxyethane Chemical compound CCOC=C FJKIXWOMBXYWOQ-UHFFFAOYSA-N 0.000 description 4
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- XPCTZQVDEJYUGT-UHFFFAOYSA-N 3-hydroxy-2-methyl-4-pyrone Chemical compound CC=1OC=CC(=O)C=1O XPCTZQVDEJYUGT-UHFFFAOYSA-N 0.000 description 2
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- 238000007796 conventional method Methods 0.000 description 2
- OXBLHERUFWYNTN-UHFFFAOYSA-M copper(I) chloride Chemical compound [Cu]Cl OXBLHERUFWYNTN-UHFFFAOYSA-M 0.000 description 2
- 239000002537 cosmetic Substances 0.000 description 2
- 239000012043 crude product Substances 0.000 description 2
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- 238000000746 purification Methods 0.000 description 2
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- 239000000243 solution Substances 0.000 description 2
- 239000001069 triethyl citrate Substances 0.000 description 2
- VMYFZRTXGLUXMZ-UHFFFAOYSA-N triethyl citrate Natural products CCOC(=O)C(O)(C(=O)OCC)C(=O)OCC VMYFZRTXGLUXMZ-UHFFFAOYSA-N 0.000 description 2
- 235000013769 triethyl citrate Nutrition 0.000 description 2
- 239000000341 volatile oil Substances 0.000 description 2
- PHXATPHONSXBIL-UHFFFAOYSA-N xi-gamma-Undecalactone Chemical compound CCCCCCCC1CCC(=O)O1 PHXATPHONSXBIL-UHFFFAOYSA-N 0.000 description 2
- NOOLISFMXDJSKH-UTLUCORTSA-N (+)-Neomenthol Chemical compound CC(C)[C@@H]1CC[C@@H](C)C[C@@H]1O NOOLISFMXDJSKH-UTLUCORTSA-N 0.000 description 1
- ORHSGDMSYGKJJY-SAIIYOCFSA-N (1'r,6's)-2,2,4',7',7'-pentamethylspiro[1,3-dioxane-5,5'-bicyclo[4.1.0]heptane] Chemical compound C12([C@H]3[C@H](C3(C)C)CCC2C)COC(C)(C)OC1 ORHSGDMSYGKJJY-SAIIYOCFSA-N 0.000 description 1
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- 238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 1
- 229920001542 oligosaccharide Polymers 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 239000012074 organic phase Substances 0.000 description 1
- 239000000546 pharmaceutical excipient Substances 0.000 description 1
- 229940067107 phenylethyl alcohol Drugs 0.000 description 1
- 239000001738 pogostemon cablin oil Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000002953 preparative HPLC Methods 0.000 description 1
- 239000012264 purified product Substances 0.000 description 1
- 235000019719 rose oil Nutrition 0.000 description 1
- 239000010666 rose oil Substances 0.000 description 1
- 229930007790 rose oxide Natural products 0.000 description 1
- 239000010671 sandalwood oil Substances 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000002453 shampoo Substances 0.000 description 1
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 1
- 230000000707 stereoselective effect Effects 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-N succinic acid Chemical compound OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 229940116411 terpineol Drugs 0.000 description 1
- LFSYLMRHJKGLDV-UHFFFAOYSA-N tetradecanolide Natural products O=C1CCCCCCCCCCCCCO1 LFSYLMRHJKGLDV-UHFFFAOYSA-N 0.000 description 1
- CRDAMVZIKSXKFV-UHFFFAOYSA-N trans-Farnesol Natural products CC(C)=CCCC(C)=CCCC(C)=CCO CRDAMVZIKSXKFV-UHFFFAOYSA-N 0.000 description 1
- MWOOGOJBHIARFG-UHFFFAOYSA-N vanillin Chemical compound COC1=CC(C=O)=CC=C1O MWOOGOJBHIARFG-UHFFFAOYSA-N 0.000 description 1
- FGQOOHJZONJGDT-UHFFFAOYSA-N vanillin Natural products COC1=CC(O)=CC(C=O)=C1 FGQOOHJZONJGDT-UHFFFAOYSA-N 0.000 description 1
- 235000012141 vanillin Nutrition 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 239000010457 zeolite 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
- C11B9/0026—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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C47/00—Compounds having —CHO groups
- C07C47/20—Unsaturated compounds having —CHO groups bound to acyclic carbon atoms
- C07C47/225—Unsaturated compounds having —CHO groups bound to acyclic carbon atoms containing rings other than six-membered aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/06—Systems containing only non-condensed rings with a five-membered ring
- C07C2601/08—Systems containing only non-condensed rings with a five-membered ring the ring being saturated
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)
- Fats And Perfumes (AREA)
- Cosmetics (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Detergent Compositions (AREA)
Abstract
Description
式中、Rはメチルまたはエチルである、
の化合物のフレーバーまたはフレグランスとしての使用が提供される。
− 精油および抽出物、例えば、カストリウム、コスタス根油、オークモスアブソリュート、ゼラニウム油、ツリーモスアブソリュート、バジル油、ベルガモット油およびマンダリン油などのフルーツ油、ギンバイカ油、パルマローザ油、パチョリ油、プチグレン油、ジャスミン油、バラ油、ビャクダン油、ワームウッド油、ラベンダー油またはイランイラン油;
− エステルおよびラクトン、例えば、ベンジルアセテート、セドリルアセテート、γ−デカラクトン、Helvetolide(登録商標)、γ−ウンデカラクトン、ベチベリルアセテート;
− 複素環、例えば、イソブチルキノリン。
a)少なくとも1つの式(I)の化合物をにおい物質として;および
b)消費者製品ベース
を含む芳香製品も提供する。
したがって、本願発明は、さらなる側面において、式(I)
の化合物に言及する。
例に記載された全ての生成物は、3−メチルシクロペンタ−2−エノン(1)から出発して取得され、ジアステレオマーまたはE/Z異性体のラセミ混合物である。
a) 3,3−ジメチルシクロペンタノン(2a)
反応器を3−メチルシクロペンタ−2−エノン(1、 150g、1.56mol)およびTHF(1.6l)で充満させ、CuCl2(2g、0.02mol)を添加した。溶液を10℃まで冷却し、THF(520ml、1.56mol)中のMeMgCl 3Mを1時間かけて滴加した。混合物を室温まで加温し30分間撹拌した。反応混合物をNH4Cl水溶液(25%、300g)に注ぎ、混合物を激しく撹拌した。NH3水溶液(25%、50ml)を添加し、撹拌を30分間続けた。深青色の混合物を分液漏斗に入れ、有機層を除去した。水層をtert.−ブチルメチルエーテルで抽出した(2×100ml)。組み合わせた有機層を塩水(200ml)で洗浄し、真空で濃縮した。残渣を20cmビグリューカラム(12Torrでの沸点80℃)での蒸留により精製し、2a(78g、45%収率)を無色の液体として得た。
反応器をビニルマグネシウムブロミド(THF中0.6M、245ml、147mmol)で充満させ、溶液を5〜10℃まで冷却した。反応混合物の温度を氷浴を用いて5〜10℃に維持しながら、THF(50ml)中3,3−ジメチルシクロペンタノン(2a、15.0g、134mmol)を10分かけて添加した。混合物を30分撹拌し、10%AcOH(150ml)で急冷し、ヘキサンで抽出した(2×100ml)。組み合わせた有機相を水で洗浄し、乾燥し(MgSO4)、濃縮し、バルブ・ツー・バルブで蒸留し、3a(14.3g、76%収率)を無色の液体として得た。
攪拌機を備えた圧力容器(PARR 4842、25ml)において、3,3−ジメチル−1−ビニルシクロペンタノール(3a、2g、14mmol)、エチルビニルエーテル(3.1g、43mmol)およびH3PO4(0.01g)の混合物を100℃(圧力2.5〜2.7bar)まで30分間加熱した。そして温度を180℃(圧力5bar)まで上げ、50分間維持した。反応混合物を真空で濃縮し、フラッシュクロマトグラフィー(エチルアセテート/ヘキサン1:9)で精製し、Ia(1.5g、E/Z異性体の1:1混合物、63%収率)を無色の液体として得た。
香りの記載(E異性体):フローラル、アルデヒド調、ウォータリー、フルーティ。
香りの記載(Z異性体):フローラル、アルデヒド調、フレッシュ、グリーン、ファッティ、ロウ様。
a) 3−エチル−3−メチルシクロペンタノン(2b)
例1aに記載したように、THF(200ml)中1mol%CuCl2の存在下で、3−メチルシクロペンタ−2−エノン(1、 35.0g、0.36mol)をエチルマグネシウムクロリド(THF中2M、218ml、0.44mol)と反応させた。粗生成物を15cmビグリューカラム(5Torrで沸点50℃)で蒸留し、2b(32.0g、69%収率)を無色の液体として得た。
例1bに記載したように、3−エチル−3−メチルシクロペンタノン(2b、30.0g、0.24mol)をビニルマグネシウムブロミド(THF中0.6M、285ml、0.29mol)と反応させ、3b(22.0g、ジアステレオマーの2:1混合物、60%収率)を無色の液体として得た。
例1cに記載したように、3−エチル−3−メチル−1−ビニルシクロペンタノール3b(8.0g、52mmol)をエチルビニルエーテルと、H3PO4(0.03g)の存在下で圧力反応器において反応した。フラッシュクロマトグラフィー(エチルアセテート/ヘキサン1:9)による粗生成物の精製により、Ib(6.0g、E/Z異性体の1:1混合物、64%収率)を無色の液体として得た。
香りの記載(E異性体):フローラル、グリーン、透明な、フリージア、アルデヒド調、樹液の多い(sappy)。
香りの記載(Z異性体):フローラル、暖かい、フルーティ、ピーチ様、葉様、スミレ。
Claims (6)
- 式(I)
の化合物。 - 4−(3,3−ジメチルシクロペンチリデン)ブタナールおよび4−(3−エチル−3−メチルシクロペンチリデン)ブタナールから選択される、請求項1に記載の化合物。
- 式(I)
の化合物のフレーバーまたはフレグランス成分としての使用。 - 式(I)
の化合物を含む、フレグランス組成物または芳香製品。 - 芳香製品が、上質な香水類、衣類のケア用品、家庭用品、美容およびパーソナルケア製品およびエアケア製品から選択される、請求項4に記載の芳香製品。
- 消費者製品ベースを改善する、増大させるまたは改変する方法であって、
これに、嗅覚が許容し得る量の式(I)
の化合物の少なくとも1種を添加する工程を含む、前記方法。
Applications Claiming Priority (3)
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GB201115409A GB201115409D0 (en) | 2011-09-07 | 2011-09-07 | Organic compounds |
GB1115409.3 | 2011-09-07 | ||
PCT/EP2012/067449 WO2013034657A1 (en) | 2011-09-07 | 2012-09-06 | Fragrance compounds and compositions |
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JP2014526571A true JP2014526571A (ja) | 2014-10-06 |
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US (1) | US9109186B2 (ja) |
EP (1) | EP2753296B1 (ja) |
JP (1) | JP6072797B2 (ja) |
CN (1) | CN103764105B (ja) |
BR (1) | BR112014005034A2 (ja) |
ES (1) | ES2550801T3 (ja) |
GB (1) | GB201115409D0 (ja) |
MX (1) | MX2014001748A (ja) |
SG (1) | SG2014005045A (ja) |
WO (1) | WO2013034657A1 (ja) |
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JP2014532065A (ja) * | 2011-10-11 | 2014-12-04 | ヴェ マン フィユV. Mane Fils | 新規シクロアルカンアルデヒド、その調製方法および香料産業におけるその使用 |
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SG11201900424SA (en) * | 2016-08-15 | 2019-02-27 | Givaudan Sa | Organic compounds |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3453317A (en) * | 1962-07-11 | 1969-07-01 | Hoffmann La Roche | Unsaturated carbonyl compounds and processes |
JPS58194832A (ja) * | 1982-05-03 | 1983-11-12 | エル・ジボ−ダン・エ・コンパニ−・ソシエテ・アノニム | 新規ケトンおよびその製造法 |
JP2001048854A (ja) * | 1999-07-05 | 2001-02-20 | Givaudan Roure Internatl Sa | シクロペンチルアルキル−ニトリル |
JP2010511677A (ja) * | 2006-12-08 | 2010-04-15 | ヴィ・マン・フィス | 香料及び香味料中の芳香成分としてのカンフォレニック誘導体の使用 |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
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DE3928242A1 (de) | 1989-08-26 | 1991-02-28 | Basf Ag | Cycloalkylidenderivate |
EP1930317A1 (en) * | 2006-12-08 | 2008-06-11 | V. Mane Fils | Use of campholenic derivatives as fragrant ingredients in perfumery and flavouring |
-
2011
- 2011-09-07 GB GB201115409A patent/GB201115409D0/en not_active Ceased
-
2012
- 2012-09-06 US US14/240,141 patent/US9109186B2/en active Active
- 2012-09-06 ES ES12762243.9T patent/ES2550801T3/es active Active
- 2012-09-06 WO PCT/EP2012/067449 patent/WO2013034657A1/en active Application Filing
- 2012-09-06 CN CN201280042894.XA patent/CN103764105B/zh not_active Expired - Fee Related
- 2012-09-06 EP EP12762243.9A patent/EP2753296B1/en active Active
- 2012-09-06 JP JP2014528979A patent/JP6072797B2/ja active Active
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- 2012-09-06 SG SG2014005045A patent/SG2014005045A/en unknown
- 2012-09-06 BR BR112014005034A patent/BR112014005034A2/pt not_active Application Discontinuation
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3453317A (en) * | 1962-07-11 | 1969-07-01 | Hoffmann La Roche | Unsaturated carbonyl compounds and processes |
JPS58194832A (ja) * | 1982-05-03 | 1983-11-12 | エル・ジボ−ダン・エ・コンパニ−・ソシエテ・アノニム | 新規ケトンおよびその製造法 |
JP2001048854A (ja) * | 1999-07-05 | 2001-02-20 | Givaudan Roure Internatl Sa | シクロペンチルアルキル−ニトリル |
JP2010511677A (ja) * | 2006-12-08 | 2010-04-15 | ヴィ・マン・フィス | 香料及び香味料中の芳香成分としてのカンフォレニック誘導体の使用 |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2014532065A (ja) * | 2011-10-11 | 2014-12-04 | ヴェ マン フィユV. Mane Fils | 新規シクロアルカンアルデヒド、その調製方法および香料産業におけるその使用 |
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EP2753296A1 (en) | 2014-07-16 |
CN103764105B (zh) | 2016-03-30 |
US9109186B2 (en) | 2015-08-18 |
ES2550801T3 (es) | 2015-11-12 |
MX2014001748A (es) | 2014-03-31 |
SG2014005045A (en) | 2014-04-28 |
WO2013034657A1 (en) | 2013-03-14 |
CN103764105A (zh) | 2014-04-30 |
BR112014005034A2 (pt) | 2017-03-21 |
US20140221263A1 (en) | 2014-08-07 |
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