5939-87-7Relevant articles and documents
Method for producing [beta]-cyclolavandulal and derivative of same
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Paragraph 0110; 0111; 0112; 0113; 0114; 0115; 0116-0118, (2016/12/22)
A given compound is synthesized simply, efficiently, and selectively. Specifically, provided are a method for producing (2,4,4-trimethyl-1-cyclohexene)carbaldehyde including at least a step for obtaining a 2,4,4-trimethyl-2-cyclohexenylidene methyl ether compound (2) by reacting the carbonyl groups of 2,4,4-trimethyl-2-cyclohexenone (1) and a step for obtaining (2,4,4-trimethyl-1-cyclohexene)carbaldehyde (3) by hydrolyzing (2), a method for producing (2,4,4-trimethyl-1-cyclohexene)methanol including at least a step for obtaining (2,4,4-trimethyl-1-cyclohexene)methanol (4) by reducing (3), and a method for producing a (2,4,4-trimethyl-1-cyclohexenyl)methyl ester compound including at least a step for obtaining a (2,4,4-trimethyl-1-cyclohexenyl)methyl ester compound (5) by esterifying (4).
An efficient synthetic method for β-cyclolavandulal and its corresponding alcohol
Oda, Mitsunori,Isobe, Atsushi,Hayashi, Masashi,Miyatake, Ryuta,Shimao, Ichiro,Kuroda, Shigeyasu
, p. 438 - 440 (2007/10/03)
3,3-Dimethylcyclohexanone (5) was efficiently converted to methyl β-cyclolavandulate (6) in 74% yield in three steps, one of which included the preparation of β-methyl α,β-unsaturated esters by coupling lithium dimethylcuprate with enol phosphates of β-ox