JP2019531266A5 - - Google Patents
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- Publication number
- JP2019531266A5 JP2019531266A5 JP2019505384A JP2019505384A JP2019531266A5 JP 2019531266 A5 JP2019531266 A5 JP 2019531266A5 JP 2019505384 A JP2019505384 A JP 2019505384A JP 2019505384 A JP2019505384 A JP 2019505384A JP 2019531266 A5 JP2019531266 A5 JP 2019531266A5
- Authority
- JP
- Japan
- Prior art keywords
- formula
- compound
- compounds
- alkyl
- ester
- 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
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- 150000001875 compounds Chemical class 0.000 claims 70
- 150000002148 esters Chemical class 0.000 claims 10
- 238000000034 method Methods 0.000 claims 9
- 125000003342 alkenyl group Chemical group 0.000 claims 8
- 125000000217 alkyl group Chemical group 0.000 claims 8
- 150000002576 ketones Chemical class 0.000 claims 8
- 239000000203 mixture Substances 0.000 claims 7
- 239000003205 fragrance Substances 0.000 claims 5
- 229910052739 hydrogen Inorganic materials 0.000 claims 4
- 239000001257 hydrogen Substances 0.000 claims 4
- 239000002184 metal Substances 0.000 claims 4
- 150000002763 monocarboxylic acids Chemical class 0.000 claims 4
- 229920006395 saturated elastomer Polymers 0.000 claims 4
- 150000002431 hydrogen Chemical class 0.000 claims 3
- 239000000126 substance Substances 0.000 claims 3
- -1 1,2,2,6-tetramethylcyclohexyl Chemical group 0.000 claims 2
- 244000166124 Eucalyptus globulus Species 0.000 claims 2
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 claims 2
- 238000006640 acetylation reaction Methods 0.000 claims 2
- 239000000796 flavoring agent Substances 0.000 claims 2
- 235000019634 flavors Nutrition 0.000 claims 2
- 238000005984 hydrogenation reaction Methods 0.000 claims 2
- 239000012038 nucleophile Substances 0.000 claims 2
- DSSYKIVIOFKYAU-XCBNKYQSSA-N (R)-camphor Chemical compound C1C[C@@]2(C)C(=O)C[C@@H]1C2(C)C DSSYKIVIOFKYAU-XCBNKYQSSA-N 0.000 claims 1
- 241000218645 Cedrus Species 0.000 claims 1
- 241000723346 Cinnamomum camphora Species 0.000 claims 1
- 241000207199 Citrus Species 0.000 claims 1
- 241000597000 Freesia Species 0.000 claims 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
- 241000212322 Levisticum officinale Species 0.000 claims 1
- 241000218657 Picea Species 0.000 claims 1
- 238000005882 aldol condensation reaction Methods 0.000 claims 1
- 150000008064 anhydrides Chemical class 0.000 claims 1
- 229960000846 camphor Drugs 0.000 claims 1
- 229930008380 camphor Natural products 0.000 claims 1
- 150000001735 carboxylic acids Chemical class 0.000 claims 1
- 238000009903 catalytic hydrogenation reaction Methods 0.000 claims 1
- 239000003153 chemical reaction reagent Substances 0.000 claims 1
- 239000003638 chemical reducing agent Substances 0.000 claims 1
- 235000020971 citrus fruits Nutrition 0.000 claims 1
- 235000009508 confectionery Nutrition 0.000 claims 1
- 239000002537 cosmetic Substances 0.000 claims 1
- 239000003599 detergent Substances 0.000 claims 1
- 239000003085 diluting agent Substances 0.000 claims 1
- 235000011869 dried fruits Nutrition 0.000 claims 1
- 230000002708 enhancing effect Effects 0.000 claims 1
- 150000004820 halides Chemical class 0.000 claims 1
- 239000001645 levisticum officinale Substances 0.000 claims 1
- 239000003446 ligand Substances 0.000 claims 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 claims 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 1
- 230000001590 oxidative effect Effects 0.000 claims 1
- 239000002304 perfume Substances 0.000 claims 1
- 239000008194 pharmaceutical composition Substances 0.000 claims 1
- 238000007363 ring formation reaction Methods 0.000 claims 1
- 239000010902 straw Substances 0.000 claims 1
- 230000002194 synthesizing effect Effects 0.000 claims 1
- 0 CC(*)C1(C)C(C)(*)CCCC1C Chemical compound CC(*)C1(C)C(C)(*)CCCC1C 0.000 description 1
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IN201621026655 | 2016-08-04 | ||
| IN201621026655 | 2016-08-04 | ||
| EP16188975 | 2016-09-15 | ||
| EP16188975.3 | 2016-09-15 | ||
| PCT/EP2017/069637 WO2018024820A1 (en) | 2016-08-04 | 2017-08-03 | 1-hydroxymethyl-1,2,2,6-tetramethyl-cyclohexane and derivatives thereof and their use as aroma chemicals |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2019531266A JP2019531266A (ja) | 2019-10-31 |
| JP2019531266A5 true JP2019531266A5 (cg-RX-API-DMAC10.html) | 2020-09-10 |
| JP6974432B2 JP6974432B2 (ja) | 2021-12-01 |
Family
ID=59677204
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2019505384A Active JP6974432B2 (ja) | 2016-08-04 | 2017-08-03 | １−ヒドロキシメチル−１，２，２，６−テトラメチル−シクロヘキサン及びその誘導体、並びにそれらのアロマケミカルとしての使用 |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US20190169108A1 (cg-RX-API-DMAC10.html) |
| EP (1) | EP3494103B1 (cg-RX-API-DMAC10.html) |
| JP (1) | JP6974432B2 (cg-RX-API-DMAC10.html) |
| CN (1) | CN109790092B (cg-RX-API-DMAC10.html) |
| BR (1) | BR112019002053B1 (cg-RX-API-DMAC10.html) |
| ES (1) | ES2902871T3 (cg-RX-API-DMAC10.html) |
| MX (1) | MX2019001393A (cg-RX-API-DMAC10.html) |
| PL (1) | PL3494103T3 (cg-RX-API-DMAC10.html) |
| WO (1) | WO2018024820A1 (cg-RX-API-DMAC10.html) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2018172109A1 (en) | 2017-03-20 | 2018-09-27 | Basf Se | Process for preparing bromotrichloromethane |
| PL3619189T3 (pl) | 2017-05-06 | 2023-01-16 | Basf Se | Octan 2,3,7-trimetylokt-6-enylu i octan 3,7-dimetylo-2-metyleno-okt-6-enylu oraz ich pochodne oraz ich zastosowanie jako substancji aromatowych |
| CN111448180B (zh) | 2017-12-18 | 2023-08-15 | 巴斯夫欧洲公司 | 通过烯酮化合物制备乙酸酯化合物 |
| JP7872796B2 (ja) * | 2021-09-30 | 2026-06-10 | クミアイ化学工業株式会社 | アルデヒド化合物及びジヒドロイソキサゾール化合物の製造方法 |
| GB202114238D0 (en) | 2021-10-05 | 2021-11-17 | Givaudan Sa | Organic compounds |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3874511T2 (de) * | 1988-01-14 | 1993-02-04 | Firmenich & Cie | Verfahren zur herstellung von cycloaliphatischen aldehyden. |
| JP2759546B2 (ja) | 1990-05-21 | 1998-05-28 | 高砂香料工業株式会社 | （３ｓ）―３，７―ジメチル―２―メチレン―６―オクテン―１―アール及びその製法並びにこれを含有する香料組成物 |
| JP2748184B2 (ja) * | 1990-09-10 | 1998-05-06 | 高砂香料工業株式会社 | 光学活性１‐（２，２，６‐トリメチルシクロヘキシル）‐２‐ブテン‐１‐オンの製造方法及びこれを含有する香料組成物 |
| JPH04283527A (ja) | 1991-03-12 | 1992-10-08 | Daicel Chem Ind Ltd | １−メチルテトラヒドロベンジルアルコ―ルの製造方法 |
| US9133082B2 (en) | 2011-06-14 | 2015-09-15 | Bikam Pharmaceuticals, Inc. | Opsin-binding ligands, compositions and methods of use |
| MX2016012467A (es) * | 2014-03-26 | 2016-12-20 | Procter & Gamble | Sistemas de perfume. |
-
2017
- 2017-08-03 MX MX2019001393A patent/MX2019001393A/es unknown
- 2017-08-03 ES ES17754650T patent/ES2902871T3/es active Active
- 2017-08-03 US US16/322,274 patent/US20190169108A1/en not_active Abandoned
- 2017-08-03 CN CN201780048197.8A patent/CN109790092B/zh active Active
- 2017-08-03 WO PCT/EP2017/069637 patent/WO2018024820A1/en not_active Ceased
- 2017-08-03 PL PL17754650T patent/PL3494103T3/pl unknown
- 2017-08-03 EP EP17754650.4A patent/EP3494103B1/en active Active
- 2017-08-03 JP JP2019505384A patent/JP6974432B2/ja active Active
- 2017-08-03 BR BR112019002053-5A patent/BR112019002053B1/pt active IP Right Grant
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