ES2721530T3 - Uso de acetato de cis- o trans-(2-isobutil-4-metil-tetrahidropiran-4-ilo) isoméricamente puro o altamente enriquecido con isómeros - Google Patents

Uso de acetato de cis- o trans-(2-isobutil-4-metil-tetrahidropiran-4-ilo) isoméricamente puro o altamente enriquecido con isómeros Download PDF

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Publication number
ES2721530T3
ES2721530T3 ES15767522T ES15767522T ES2721530T3 ES 2721530 T3 ES2721530 T3 ES 2721530T3 ES 15767522 T ES15767522 T ES 15767522T ES 15767522 T ES15767522 T ES 15767522T ES 2721530 T3 ES2721530 T3 ES 2721530T3
Authority
ES
Spain
Prior art keywords
isobutyl
acetate
methyl
tetrahydropyran
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.)
Active
Application number
ES15767522T
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English (en)
Spanish (es)
Inventor
Timon Stork
Stefan Rüdenauer
Margarethe Klos
Ralf Pelzer
Wolfgang Krause
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
BASF SE
Original Assignee
BASF SE
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by BASF SE filed Critical BASF SE
Application granted granted Critical
Publication of ES2721530T3 publication Critical patent/ES2721530T3/es
Active legal-status Critical Current
Anticipated expiration legal-status Critical

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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
    • C11B9/0069—Heterocyclic compounds
    • C11B9/0073—Heterocyclic compounds containing only O or S as heteroatoms
    • C11B9/008—Heterocyclic compounds containing only O or S as heteroatoms the hetero rings containing six atoms
    • A—HUMAN NECESSITIES
    • A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23L—FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES, NOT OTHERWISE PROVIDED FOR; PREPARATION OR TREATMENT THEREOF
    • A23L27/00—Spices; Flavouring agents or condiments; Artificial sweetening agents; Table salts; Dietetic salt substitutes; Preparation or treatment thereof
    • A23L27/20—Synthetic spices, flavouring agents or condiments
    • A23L27/205—Heterocyclic compounds
    • A23L27/2052—Heterocyclic compounds having oxygen or sulfur as the only hetero atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D309/00—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings
    • C07D309/02—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
    • C07D309/08—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D309/10—Oxygen atoms

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Food Science & Technology (AREA)
  • Polymers & Plastics (AREA)
  • Nutrition Science (AREA)
  • Health & Medical Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Wood Science & Technology (AREA)
  • Fats And Perfumes (AREA)
  • Cosmetics (AREA)
  • Seasonings (AREA)
  • Pyrane Compounds (AREA)
  • Medicinal Preparation (AREA)
  • Detergent Compositions (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
ES15767522T 2014-09-26 2015-09-25 Uso de acetato de cis- o trans-(2-isobutil-4-metil-tetrahidropiran-4-ilo) isoméricamente puro o altamente enriquecido con isómeros Active ES2721530T3 (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP14186627 2014-09-26
PCT/EP2015/072083 WO2016046360A1 (de) 2014-09-26 2015-09-25 Verwendung von isomerenreinem oder hoch isomerenangereichertem cis- oder trans-(2-isobutyl-4-methyl-tetrahydropyran-4-yl)acetat

Publications (1)

Publication Number Publication Date
ES2721530T3 true ES2721530T3 (es) 2019-08-01

Family

ID=51752982

Family Applications (1)

Application Number Title Priority Date Filing Date
ES15767522T Active ES2721530T3 (es) 2014-09-26 2015-09-25 Uso de acetato de cis- o trans-(2-isobutil-4-metil-tetrahidropiran-4-ilo) isoméricamente puro o altamente enriquecido con isómeros

Country Status (9)

Country Link
US (1) US10160931B2 (https=)
EP (1) EP3197987B1 (https=)
JP (1) JP6822948B2 (https=)
CN (1) CN106715408B (https=)
ES (1) ES2721530T3 (https=)
MX (1) MX375962B (https=)
PL (1) PL3197987T3 (https=)
TR (1) TR201904599T4 (https=)
WO (1) WO2016046360A1 (https=)

Families Citing this family (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP6741687B2 (ja) 2015-05-04 2020-08-19 ビーエーエスエフ ソシエタス・ヨーロピアＢａｓｆ Ｓｅ メロナールの調製方法
BR112018000481B1 (pt) 2015-07-10 2022-01-11 Basf Se Processos para preparação de compostos e de (-)- ambrox (v)
CN107848929A (zh) 2015-07-15 2018-03-27 巴斯夫欧洲公司 制备芳基丙烯的方法
US10202323B2 (en) 2015-07-15 2019-02-12 Basf Se Process for preparing an arylpropene
EP3170828A1 (de) 2015-11-23 2017-05-24 Basf Se Verfahren zur herstellung von verbindungen mit 16-oxabicyclo[10.3.1]pentadecengerüst und deren folgeprodukten
ES2899827T3 (es) 2015-12-08 2022-03-14 Basf Se Material zeolítico que contiene estaño y que tiene una estructura de marco BEA
EP3816297A1 (de) 2016-02-19 2021-05-05 Basf Se Biokatalytische zyklisierung von mehrfach ungesättigten carbonsäuren-verbindungen
US10981885B2 (en) 2016-05-31 2021-04-20 Basf Se Tetrahydropyranyl lower alkyl esters and the production of same using a ketene compound
WO2017211784A1 (en) 2016-06-07 2017-12-14 Basf Se Process for preparing 2,3-unsaturated alcohols
JP7039551B2 (ja) 2016-07-15 2022-03-22 ビーエーエスエフ ソシエタス・ヨーロピア ３－メチル－１，５－シクロペンタデカンジオンからの１４－メチル－１６－オキサビシクロ［１０．３．１］ペンタデセンの調製
EP3572487A1 (en) * 2018-05-25 2019-11-27 Basf Se 2-furyl- and 2-thienyl-substituted di- and tetrahydropyrans for use as aroma chemicals
EP3880777B1 (en) * 2018-11-13 2025-06-25 Symrise AG Perfuming ingredients with lily of the valley note
EP3838895A1 (en) * 2019-12-16 2021-06-23 Basf Se Substituted 4-methylene-tetrahydropyrans, 4-methyl-dihydropyrans and 4-methyl-tetrahydropyrans and use thereof as aroma chemicals
CN119790128A (zh) * 2022-09-06 2025-04-08 西姆莱斯股份公司 香料混合物(iii)

Family Cites Families (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4963285A (en) * 1989-02-09 1990-10-16 International Flavors & Fragrances Inc. 2,4,4-irisubstituted tetrahydro pyranyl esters and organoleptic uses thereof
EP2432773B1 (de) 2009-05-19 2013-08-28 Basf Se Verfahren zur Herstellung von 2-substituierten Tetrahydropyranolen
MX2012013509A (es) 2010-05-27 2013-01-24 Basf Se Procedimiento para la preparacion de tetrahidropiranoles 2-sustituidos.
ES2511143T3 (es) 2010-06-10 2014-10-22 Basf Se Procedimiento para la preparación y aislamiento de tetrahidropiranoles sustituidos en la posición 2
ES2498942T3 (es) * 2010-11-10 2014-09-26 Basf Se Composiciones de perfume que comprenden mezclas especiales de diastereómeros de 2-isobutil-4-metil-tetrahidro-2H-piran-4-ol
US9340754B2 (en) 2012-11-27 2016-05-17 Basf Se Process for the preparation of cyclohexyl-substituted tertiary alkanols
ES2676411T3 (es) 2013-04-29 2018-07-19 Basf Se Procedimiento para la preparación de 4-hidroxi-4-metil-tetrahidropiranos 2-sustituidos, con recirculación
CN106103398A (zh) 2014-01-17 2016-11-09 巴斯夫欧洲公司 用于生产芳基丙烯的方法
EP3131888B1 (de) 2014-04-14 2022-08-03 Basf Se Herstellung von 2-substituierten 4-hydroxy-4-methyl-tetrahydropyranen aus 2-alkyl-4,4-dimethyl-1,3-dioxan-haltigen ausgangsstoffen
EP2865676A1 (de) 2014-04-14 2015-04-29 Basf Se Herstellung von 2-substituierten 4-Methyl-tetrahydropyranen aus 2-Alkyl-4,4-dimethyl-1,3-dioxan-haltigen Ausgangsstoffen
MX386539B (es) 2014-04-14 2025-03-18 Basf Se Producción de 4-hidroxi-4-metiltetrahidropiranos 2-sustituidos que tienen calidad odorífera estable.
US20170275225A1 (en) 2014-09-09 2017-09-28 Basf Se Method for the preparation of 2-alkoxy cyclohexanol
CN106660916A (zh) 2014-09-09 2017-05-10 巴斯夫欧洲公司 生产芳香物质的方法

Also Published As

Publication number Publication date
EP3197987B1 (de) 2019-01-23
JP6822948B2 (ja) 2021-01-27
MX2017003923A (es) 2017-06-30
JP2017530126A (ja) 2017-10-12
US10160931B2 (en) 2018-12-25
WO2016046360A1 (de) 2016-03-31
TR201904599T4 (tr) 2019-04-22
CN106715408B (zh) 2020-06-09
PL3197987T3 (pl) 2019-07-31
MX375962B (es) 2025-03-06
US20170292084A1 (en) 2017-10-12
CN106715408A (zh) 2017-05-24
EP3197987A1 (de) 2017-08-02

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