(R)-(1,4-dioxa-8-azspiro<4.5>dec-8-yl)(3-phenylcyclohex-3-enyl)methanone

Base Information

Chemical Name:(R)-(1,4-dioxa-8-azspiro<4.5>dec-8-yl)(3-phenylcyclohex-3-enyl)methanone
CAS No.:1026841-38-2
Molecular Formula:C₂₀H₂₅NO₃
Molecular Weight:327.423
Hs Code.:

Synonyms:(R)-(1,4-dioxa-8-azspiro<4.5>dec-8-yl)(3-phenylcyclohex-3-enyl)methanone

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of (R)-(1,4-dioxa-8-azspiro<4.5>dec-8-yl)(3-phenylcyclohex-3-enyl)methanone

Chemical Property:

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Technology Process of (R)-(1,4-dioxa-8-azspiro<4.5>dec-8-yl)(3-phenylcyclohex-3-enyl)methanone

There total 1 articles about (R)-(1,4-dioxa-8-azspiro<4.5>dec-8-yl)(3-phenylcyclohex-3-enyl)methanone 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:

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

: 150013-81-3
(R)-(+)-3-phenyl-3-cyclohexenecarboxylic acid

: 1026841-38-2
(R)-(1,4-dioxa-8-azspiro<4.5>dec-8-yl)(3-phenylcyclohex-3-enyl)methanone

Guidance literature:: With triethylamine; isobutyl chloroformate; Yield given. Multistep reaction; 1.) CH₂Cl₂, -20 deg C, 30 min, 2.) CH₂Cl₂, 25 deg C, overnight;

Reference yield:

: 1026841-38-2
(R)-(1,4-dioxa-8-azspiro<4.5>dec-8-yl)(3-phenylcyclohex-3-enyl)methanone

: 1027045-39-1
8-((R)-3-Phenyl-cyclohex-3-enylmethyl)-1,4-dioxa-8-aza-spiro[4.5]decane

Guidance literature:: With lithium aluminium tetrahydride; aluminium trichloride; In tetrahydrofuran; diethyl ether; at 0 ℃; for 2h;

Reference yield:

: 1026841-38-2
(R)-(1,4-dioxa-8-azspiro<4.5>dec-8-yl)(3-phenylcyclohex-3-enyl)methanone

: 1027314-63-1
(R)-1-<(3-phenylcyclohex-3-enyl)methyl>piperidin-4-one

Guidance literature:: Multi-step reaction with 2 steps

1: AlCl₃, LiAlH₄ / tetrahydrofuran; diethyl ether / 2 h / 0 °C

2: 2 N HCl / tetrahydrofuran / 2 h / Heating

With hydrogenchloride; lithium aluminium tetrahydride; aluminium trichloride; In tetrahydrofuran; diethyl ether;