6-ethoxy-8-cyclohexyl-6-oxo-3(S),5-diphenyl-1-oxa-4-aza-6-phosphabicyclo[3.3.0]octane

Base Information

Chemical Name:6-ethoxy-8-cyclohexyl-6-oxo-3(S),5-diphenyl-1-oxa-4-aza-6-phosphabicyclo[3.3.0]octane
CAS No.:1333841-08-9
Molecular Formula:C₂₅H₃₂NO₃P
Molecular Weight:425.508
Hs Code.:

Synonyms:6-ethoxy-8-cyclohexyl-6-oxo-3(S),5-diphenyl-1-oxa-4-aza-6-phosphabicyclo[3.3.0]octane

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Chemical Property of 6-ethoxy-8-cyclohexyl-6-oxo-3(S),5-diphenyl-1-oxa-4-aza-6-phosphabicyclo[3.3.0]octane

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Technology Process of 6-ethoxy-8-cyclohexyl-6-oxo-3(S),5-diphenyl-1-oxa-4-aza-6-phosphabicyclo[3.3.0]octane

There total 3 articles about 6-ethoxy-8-cyclohexyl-6-oxo-3(S),5-diphenyl-1-oxa-4-aza-6-phosphabicyclo[3.3.0]octane 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: 56.0%

: 1333390-41-2
C₁₀H₁₇O₂P

: 74879-43-9
(S)-2-Phenyl-2-{[1-phenyl-meth-(E)-ylidene]-amino}-ethanol

: 1333841-08-9
6-ethoxy-8-cyclohexyl-6-oxo-3(S),5-diphenyl-1-oxa-4-aza-6-phosphabicyclo[3.3.0]octane

Guidance literature:: In acetonitrile; at 60 ℃; for 264h; Inert atmosphere;
DOI:10.1021/ol2019345

Reference yield:

: 78-27-3
1-Ethynylcyclohexan-1-ol

: 1333841-08-9
6-ethoxy-8-cyclohexyl-6-oxo-3(S),5-diphenyl-1-oxa-4-aza-6-phosphabicyclo[3.3.0]octane

Guidance literature:: Multi-step reaction with 3 steps

1: hypophosphorous acid / toluene / Reflux

2: chloroform / 70 °C

3: acetonitrile / 264 h / 60 °C / Inert atmosphere

With hypophosphorous acid; In chloroform; toluene; acetonitrile;
DOI:10.1021/ol2019345

Reference yield:

: (2-cyclohexylidenevinyl)phosphinic acid

: 1333841-08-9
6-ethoxy-8-cyclohexyl-6-oxo-3(S),5-diphenyl-1-oxa-4-aza-6-phosphabicyclo[3.3.0]octane

Guidance literature:: Multi-step reaction with 2 steps

1: chloroform / 70 °C

2: acetonitrile / 264 h / 60 °C / Inert atmosphere

In chloroform; acetonitrile;
DOI:10.1021/ol2019345