2-<(tert-butyloxy)carbonyl>-6-<2-(p-phenylphenoxy)ethyl>-8-methyl-3,7-dioxo-1-azabicyclo<4.1.1>octane

Base Information

Chemical Name:2-<(tert-butyloxy)carbonyl>-6-<2-(p-phenylphenoxy)ethyl>-8-methyl-3,7-dioxo-1-azabicyclo<4.1.1>octane
CAS No.:118248-81-0
Molecular Formula:C₂₇H₃₁NO₅
Molecular Weight:449.547
Hs Code.:

Synonyms:2-<(tert-butyloxy)carbonyl>-6-<2-(p-phenylphenoxy)ethyl>-8-methyl-3,7-dioxo-1-azabicyclo<4.1.1>octane

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Chemical Property of 2-<(tert-butyloxy)carbonyl>-6-<2-(p-phenylphenoxy)ethyl>-8-methyl-3,7-dioxo-1-azabicyclo<4.1.1>octane

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Technology Process of 2-<(tert-butyloxy)carbonyl>-6-<2-(p-phenylphenoxy)ethyl>-8-methyl-3,7-dioxo-1-azabicyclo<4.1.1>octane

There total 8 articles about 2-<(tert-butyloxy)carbonyl>-6-<2-(p-phenylphenoxy)ethyl>-8-methyl-3,7-dioxo-1-azabicyclo<4.1.1>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: 50.0%

: 5-{(2S,3R)-3-[2-(Biphenyl-4-yloxy)-ethyl]-2-methyl-4-oxo-azetidin-3-yl}-2-diazo-3-oxo-pentanoic acid tert-butyl ester

: 118248-81-0
2-<(tert-butyloxy)carbonyl>-6-<2-(p-phenylphenoxy)ethyl>-8-methyl-3,7-dioxo-1-azabicyclo<4.1.1>octane

Guidance literature:: With dirhodium tetraacetate; In benzene;
DOI:10.1021/ja00185a043

Reference yield:

: 118269-65-1
3-(2'-hydroxyethyl)-3-(3'-butenyl)-4-methylazetidin-2-one

: 118248-81-0
2-<(tert-butyloxy)carbonyl>-6-<2-(p-phenylphenoxy)ethyl>-8-methyl-3,7-dioxo-1-azabicyclo<4.1.1>octane

Guidance literature:: Multi-step reaction with 6 steps

1: PPh₃/DEAD

2: 1.) O₃, 2.) Me₂S / 1.) MeOH, -78 deg C, 2.) -78 deg C to room temp.

3: Jones reagent (8N) / acetone / 0 °C

4: 1.) N,N'-carbonyldiimidazole / 1.) THF, room temp.

5: tosyl azide, triethylamine / acetonitrile / Ambient temperature

6: 50 percent / Rh₂(OAc)4 / benzene

With dirhodium tetraacetate; 4-toluenesulfonyl azide; dimethylsulfide; Jones reagent (8N); ozone; triethylamine; triphenylphosphine; 1,1'-carbonyldiimidazole; diethylazodicarboxylate; In acetone; acetonitrile; benzene;
DOI:10.1021/ja00185a043

Reference yield:

: 118248-73-0
(3S,4R)-3-[2-(Biphenyl-4-yloxy)-ethyl]-3-but-3-enyl-4-methyl-azetidin-2-one

: 118248-81-0
2-<(tert-butyloxy)carbonyl>-6-<2-(p-phenylphenoxy)ethyl>-8-methyl-3,7-dioxo-1-azabicyclo<4.1.1>octane

Guidance literature:: Multi-step reaction with 5 steps

1: 1.) O₃, 2.) Me₂S / 1.) MeOH, -78 deg C, 2.) -78 deg C to room temp.

2: Jones reagent (8N) / acetone / 0 °C

3: 1.) N,N'-carbonyldiimidazole / 1.) THF, room temp.

4: tosyl azide, triethylamine / acetonitrile / Ambient temperature

5: 50 percent / Rh₂(OAc)4 / benzene

With dirhodium tetraacetate; 4-toluenesulfonyl azide; dimethylsulfide; Jones reagent (8N); ozone; triethylamine; 1,1'-carbonyldiimidazole; In acetone; acetonitrile; benzene;
DOI:10.1021/ja00185a043