Processes for preparing alpha-necrodyl compounds and processes for preparing gamma-necrodyl compounds
AssigneeShin-Etsu Chemical Co., Ltd.
InventorsTomohiro Watanabe, Takeshi Kinsho, Yusuke Nagae
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AssigneeShin-Etsu Chemical Co., Ltd.
InventorsTomohiro Watanabe, Takeshi Kinsho, Yusuke Nagae
Estimating the term…
The present invention provides processes for preparing an α-necrodyl compound of the following general formula (3): wherein R2 represents a monovalent hydrocarbon group having 1 to 9 carbon atoms, the process comprising: subjecting a 3, 5, 5-trimethyl-3-cyclopentene compound of the following general formula (1): wherein R2 is as defined above, and X represents a leaving group, to a nucleophilic substitution reaction with a methylating agent of the following general formula (2): wherein M represents Li, MgZ1, ZnZ1, Cu, CuZ1, or CuLiZ1, and Z1 represents a halogen atom or a methyl group, to form the α-necrodyl compound (3). The present invention further provides processes for preparing γ-necrodyl compounds of the following general formula (4): wherein R2 represents a monovalent hydrocarbon group having 1 to 9 carbon atoms, the process comprising: subjecting the α-necrodyl compound (3) thus obtained to a positional isomerization reaction at the double bond to form the γ-necrodyl compound (4).
A process for preparing an α-necrodyl compound of the following general formula (3):
(2-Hydroxy-3, 5, 5-trimethyl-3-cyclopentenyl)methanol of the following formula (5):
Dependencies are inferred from the claim text.