7-(3-cyanopropyl)-8-phenyl-1,4-dioxa-8-azaspiro[4.5]decane-7-carbonitrile

Base Information

Chemical Name:7-(3-cyanopropyl)-8-phenyl-1,4-dioxa-8-azaspiro[4.5]decane-7-carbonitrile
CAS No.:859499-51-7
Molecular Formula:C₁₈H₂₁N₃O₂
Molecular Weight:311.384
Hs Code.:

Synonyms:

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Chemical Property of 7-(3-cyanopropyl)-8-phenyl-1,4-dioxa-8-azaspiro[4.5]decane-7-carbonitrile

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Technology Process of 7-(3-cyanopropyl)-8-phenyl-1,4-dioxa-8-azaspiro[4.5]decane-7-carbonitrile

There total 4 articles about 7-(3-cyanopropyl)-8-phenyl-1,4-dioxa-8-azaspiro[4.5]decane-7-carbonitrile 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:

: 859499-49-3
8-phenyl-1,4-dioxa-8-azaspiro[4.5]decane-7-carbonitrile

: 859499-51-7
7-(3-cyanopropyl)-8-phenyl-1,4-dioxa-8-azaspiro[4.5]decane-7-carbonitrile

Guidance literature:: Multi-step reaction with 2 steps

1.1: LDA / tetrahydrofuran; cyclohexane / 1 h / -40 °C

1.2: 94 percent / tetrahydrofuran; cyclohexane / 12 h / -20 °C

2.1: 84 percent / tetrabutylammonium iodide / dimethylsulfoxide / 48 h / 20 °C

With tetra-(n-butyl)ammonium iodide; lithium diisopropyl amide; In tetrahydrofuran; cyclohexane; dimethyl sulfoxide;
DOI:10.1002/ejoc.200400846

Reference yield:

: 108-86-1,52753-63-6
bromobenzene

: 859499-51-7
7-(3-cyanopropyl)-8-phenyl-1,4-dioxa-8-azaspiro[4.5]decane-7-carbonitrile

Guidance literature:: Multi-step reaction with 4 steps

1.1: 74 percent / tBuOH; NaNH₂ / tetrahydrofuran / 50 °C

2.1: 70 percent / lithium acetate / methanol / Electrolysis

3.1: LDA / tetrahydrofuran; cyclohexane / 1 h / -40 °C

3.2: 94 percent / tetrahydrofuran; cyclohexane / 12 h / -20 °C

4.1: 84 percent / tetrabutylammonium iodide / dimethylsulfoxide / 48 h / 20 °C

With lithium acetate; tetra-(n-butyl)ammonium iodide; sodium amide; tert-butyl alcohol; lithium diisopropyl amide; In tetrahydrofuran; methanol; cyclohexane; dimethyl sulfoxide; 1.1: Caubere coupling;
DOI:10.1002/ejoc.200400846

Reference yield:

: 177-11-7
4,4-ethylenedioxy-piperidine

: 859499-51-7
7-(3-cyanopropyl)-8-phenyl-1,4-dioxa-8-azaspiro[4.5]decane-7-carbonitrile

Guidance literature:: Multi-step reaction with 4 steps

1.1: 74 percent / tBuOH; NaNH₂ / tetrahydrofuran / 50 °C

2.1: 70 percent / lithium acetate / methanol / Electrolysis

3.1: LDA / tetrahydrofuran; cyclohexane / 1 h / -40 °C

3.2: 94 percent / tetrahydrofuran; cyclohexane / 12 h / -20 °C

4.1: 84 percent / tetrabutylammonium iodide / dimethylsulfoxide / 48 h / 20 °C

With lithium acetate; tetra-(n-butyl)ammonium iodide; sodium amide; tert-butyl alcohol; lithium diisopropyl amide; In tetrahydrofuran; methanol; cyclohexane; dimethyl sulfoxide; 1.1: Caubere coupling;
DOI:10.1002/ejoc.200400846