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
Other languages
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)
  • Polymers & Plastics (AREA)
  • Nutrition Science (AREA)
  • Health & Medical Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Wood Science & Technology (AREA)
  • Food 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
WO2016177814A1 (en) 2015-05-04 2016-11-10 Basf Se Process for the preparation of melonal
PL3319951T3 (pl) 2015-07-10 2022-02-28 Basf Se Sposób hydroformylowania 2-podstawionych butadienów oraz wytwarzania ich produktów pochodnych, w szczególności ambroksu
WO2017009458A1 (en) 2015-07-15 2017-01-19 Basf Se Process for preparing an arylpropene
MX2018000609A (es) 2015-07-15 2018-05-07 Basf Se Proceso para preparar un arilpropeno.
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
US10737944B2 (en) 2015-12-08 2020-08-11 Basf Se Tin-containing zeolitic material having a BEA framework structure
MX380770B (es) 2016-02-19 2025-03-12 Basf Se Ciclación enzimática de ácido homofarnesílico.
MX2018014918A (es) 2016-05-31 2019-09-05 Basf Se Esteres de tetrahidropiranilalquilo inferior y su produccion usando un compuesto de ceteno.
CN109311789B (zh) 2016-06-07 2023-04-04 巴斯夫欧洲公司 制备2,3-不饱和醇的方法
CN109476577A (zh) 2016-07-15 2019-03-15 巴斯夫欧洲公司 由3-甲基-1,5-环十五烷二酮制备14-甲基-16-氧杂双环[10.3.1]十五烯
EP3572487A1 (en) * 2018-05-25 2019-11-27 Basf Se 2-furyl- and 2-thienyl-substituted di- and tetrahydropyrans for use as aroma chemicals
CN112969774B (zh) * 2018-11-13 2025-02-14 西姆莱斯有限公司 具有铃兰香味的加香成分
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
EP4584351A1 (en) * 2022-09-06 2025-07-16 Symrise AG A fragrance mixture (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
US8618315B2 (en) 2009-05-19 2013-12-31 Basf Se Method for producing 2-substituted tetrahydropyranols
ES2660768T3 (es) 2010-05-27 2018-03-26 Basf Se Procedimiento para la preparación de tetrahidropiranoles sustituidos en posición 2
MX2012014204A (es) 2010-06-10 2013-02-07 Basf Se Proceso para la preparacion y aislamiento de 2 - tetrahidropiranoles sustituidos.
MX337560B (es) * 2010-11-10 2016-03-10 Basf Se Composiciones de fragancia que comprenden mezclas especiales de diaestereomeros 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
WO2014177484A1 (de) 2013-04-29 2014-11-06 Basf Se Verfahren zur herstellung von 2-substituierten 4-hydroxy-4-methyl-tetrahydropyranen mit rückführung
ES2679594T3 (es) 2014-01-17 2018-08-29 Basf Se Procedimiento para la preparación de arilpropenos
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
JP6549611B2 (ja) 2014-04-14 2019-07-24 ビーエーエスエフ ソシエタス・ヨーロピアＢａｓｆ Ｓｅ 匂いの品質が安定した２−置換４−ヒドロキシ−４−メチルテトラヒドロピランの製造
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
WO2016038019A1 (de) 2014-09-09 2016-03-17 Basf Se Verfahren zur herstellung von 2-alkoxycyclohexanol
MX2017003133A (es) 2014-09-09 2017-06-14 Basf Se Metodo para producir una sustancia aromatica.

Also Published As

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

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