Farnesal → a Farnesol

HRID 1534332

反応式

HRID 1534332 の反応式
[CH3:1][C:2]([CH3:16])=[CH:3][CH2:4][CH2:5]/[C:6](/[CH3:15])=[CH:7]/[CH2:8][CH2:9]/[C:10](/[CH3:14])=[CH:11]/[CH:12]=[O:13].CC(=CCCC(C)=CCCC(C)=CC=O)C.CC(=CCCC(C)=CCC=C(C)C=C)C>>[OH:13][CH2:12][CH:11]=[C:10]([CH2:9][CH2:8][CH:7]=[C:6]([CH2:5][CH2:4][CH:3]=[C:2]([CH3:16])[CH3:1])[CH3:15])[CH3:14]

参加物

4

反応物 3

HCID 68150FarnesalHCID 4423683,7,11-Trimethyl-1,3,6,10-dodecatetraeneHCID 5280598(2E,6E)-3,7,11-trimethyldodeca-2,6,10-trienal

生成物 1

HCID 3327a Farnesol

実験手順

Arctander "Perfume and Flavor Chemicals (Aroma Chemicals)", at Monograph 1378, discloses "Farnesal", 2,6,10-trimethyl-2,6,10-dodecatrien-12-al to have a very mild, sweet oily, slightly woody, tenacious odor. On the other hand, Arctander also describes, at Monograph 1379, Farnesene, 2,6,10-trimethyl 2,6,9,11-dodecatetraene defined according to the structure: ##STR11## to have a very mild, sweet and warm, rather nondescript odor of good tenacity. Arctander further states that apart from some possible use in the reconstruction of certain essential oils, there is to the author's knowledge, very little, if any, use for this sesquiterpene in perfumery as such. Arctander further states that Farnesene having the structure: ##STR12## is produced by dehydration of Farnesol by heat with a potassium dehydrating agent or from Nerolidol by heat with acetic anhydride.

後処理

  1. temperaturewarm

出典と根拠

ORDレコード
ord-de9c424a25d943a68694bb5cefaa0952
出典データセット
uspto-grants-1992_02
特許番号
US05089469

関連ノート

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