77104-99-5Relevant academic research and scientific papers
Synthesis method of tert-butyl phenylpropionaldehyde
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Paragraph 0010; 0037; 0039; 0041; 0043; 0045; 0047, (2021/03/30)
The invention discloses a synthesis method of tert-butyl phenylpropionaldehyde and relates to the field of perfume raw material synthesis, the method comprises the following steps: 1) synthesis of allylidene di(acetate)(AEDA): acetic anhydride and acrolein react at a certain temperature under the action of a catalyst A to obtain AEDA, 2) synthesis of a bourgeonal(BGA) precursor: tert-butylbenzeneand AEDA react at a certain temperature under the action of a catalyst B to obtain ortho-position and para-position BGA precursors, and 3) alcoholysis on the BGA precursor to prepare the BGA: the BGAprecursor, a solvent and a catalyst C react at a certain temperature to obtain the ortho-BGA and the para-BGA. Tert-butylbenzene is used as an initial raw material, acrolein is subjected to aldehyde group protection by acetic anhydride, then condensation is performed to obtain precursors of ortho-position and para-position bordeaux aldehyde, and an ortho-position and para-position tert-butylphenylpropionaldehyde mixed product is obtained through aldehyde group protection removal by hydrolysis, and the method is simple in process, low in raw material price, less in three wastes and elegant in fragrance, and can realize mass production.
CATALYTIC SCRIABINE REACTION
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Page/Page column 5, (2008/06/13)
The present invention relates to the field of organic synthesis. More particularly it provides a process for making aromatic non-conjugated enol esters or enol ethers from an aromatic compound or moiety and a protected enal compound or moiety, such as an acetal or an acylal. The reaction is promoted by a salt of formula MX1-4, M representing a transition metal such as Zn or Fe and X representing a mono-anion, or by BY3, wherein Y represents a fluoride or a phenyl group optionally substituted.
