9-[1-(4-methoxyphenylpiperidin)-4-ylidene]-3,3-dimethyl-1,5-dioxaspiro[5.5]undecane

Base Information

Chemical Name:9-[1-(4-methoxyphenylpiperidin)-4-ylidene]-3,3-dimethyl-1,5-dioxaspiro[5.5]undecane
CAS No.:267428-50-2
Molecular Formula:C₂₃H₃₃NO₃
Molecular Weight:371.52
Hs Code.:

Synonyms:9-[1-(4-methoxyphenylpiperidin)-4-ylidene]-3,3-dimethyl-1,5-dioxaspiro[5.5]undecane

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Chemical Property of 9-[1-(4-methoxyphenylpiperidin)-4-ylidene]-3,3-dimethyl-1,5-dioxaspiro[5.5]undecane

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Technology Process of 9-[1-(4-methoxyphenylpiperidin)-4-ylidene]-3,3-dimethyl-1,5-dioxaspiro[5.5]undecane

There total 2 articles about 9-[1-(4-methoxyphenylpiperidin)-4-ylidene]-3,3-dimethyl-1,5-dioxaspiro[5.5]undecane which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 84.0%

: 267428-49-9
9-[1-(4-methoxyphenyl)-4-hydroxy-piperidin-4-yl]-3,3-dimethyl-1,5-dioxaspiro[5.5]undecane-9-carboxylic acid

: 267428-50-2
9-[1-(4-methoxyphenylpiperidin)-4-ylidene]-3,3-dimethyl-1,5-dioxaspiro[5.5]undecane

Guidance literature:: With N,N-dimethylformamide dineopentyl acetal; In acetonitrile; Heating;
DOI:10.1021/ja983716r

Reference yield:

: 169822-66-6
3,3-Dimethyl-1,5-dioxaspiro[5.5]undecane-9-carboxylic acid

: 267428-50-2
9-[1-(4-methoxyphenylpiperidin)-4-ylidene]-3,3-dimethyl-1,5-dioxaspiro[5.5]undecane

Guidance literature:: Multi-step reaction with 2 steps

1: 39 percent / LDA / tetrahydrofuran; hexane / 2 h / 50 °C

2: 84 percent / N,N-dimethylformamide dineopentyl acetal / acetonitrile / Heating

With N,N-dimethylformamide dineopentyl acetal; lithium diisopropyl amide; In tetrahydrofuran; hexane; acetonitrile; 1: Substitution / 2: Decarboxylation;
DOI:10.1021/ja983716r