Process of production of dehydrolinalyl acetate (I)
US-9505699-B2 · Nov 29, 2016 · US
US9434676B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9434676-B2 |
| Application number | US-201314432252-A |
| Country | US |
| Kind code | B2 |
| Filing date | Oct 7, 2013 |
| Priority date | Oct 8, 2012 |
| Publication date | Sep 6, 2016 |
| Grant date | Sep 6, 2016 |
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The present invention relates to the use of specific organic compounds of formula (I) as flavor and fragrance material. Furthermore the invention relates to a new specific organic compound, as well as to flavor and fragrance formulations comprising at least one of the specific organic compounds.
Opening claim text (preview).
The invention claimed is: 1. A flavor and fragrance formulation comprising at least one compound of formula (I): wherein R 1 is —OH or —O(CO)CH 3 . 2. The flavor and fragrance formulation according to claim 1 comprising 0.0001-10 wt-%, relative to the total weight of the flavor and fragrance formulation, of at least one compound of formula (I). 3. The flavor and fragrance formulation according to claim 1 , wherein the flavor and fragrance formulation is solid, gel-like or liquid. 4. The flavor and fragrance formulation according to claim 1 , wherein the flavor and fragrance formulation is a perfume, hair care product, household product, laundry product, body care product or cosmetic product. 5. A method of improving, enhancing or modifying a flavor and fragrance formulation which comprises adding to the flavor or fragrance formulation an olfactory acceptable amount of at least one compound of formula (I): wherein R 1 is —OH or —O(CO)CH 3 . 6. A compound of formula (Ib): wherein AcO represents an acetyloxy group CH 3 (CO)O—. 7. A process for the manufacture of a compound of formula (Ib): wherein AcO represents an acetyloxy group CH 3 (CO)O—, the process comprising the steps of: i) ethinylating 5,6-dimethyl-5-hepten-2-on to 3,6,7-trimethyl-6-octen-1-in-3-ol; ii) acylating 3,6,7-trimethyl-6-octen-1-in-3-ol to 3,6,7-trimethyl-6-octen-1-in-3-yl acetate; and iii) hydrogenating the C≡C triple bond of 3,6,7-trimethyl-6-octen-1-in-3-yl acetate to the saturated C—C bond in the presence of a Lindlar catalyst leading to the compound of formula (Ib).
Hydroxy compounds · CPC title
Carboxy compounds · CPC title
Perfumes · CPC title
Alcohols having more than seven atoms in an unbroken chain · CPC title
Esters of carboxylic acids · CPC title
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