(6R)-1-aza-6-[(tert-butyldimethylsiloxy)methyl]-4-phenyl-2-oxobicyclo[4.3.0]nonane

Base Information

Chemical Name:(6R)-1-aza-6-[(tert-butyldimethylsiloxy)methyl]-4-phenyl-2-oxobicyclo[4.3.0]nonane
CAS No.:325460-66-0
Molecular Formula:C₂₁H₃₃NO₂Si
Molecular Weight:359.584
Hs Code.:

Synonyms:(6R)-1-aza-6-[(tert-butyldimethylsiloxy)methyl]-4-phenyl-2-oxobicyclo[4.3.0]nonane

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Chemical Property of (6R)-1-aza-6-[(tert-butyldimethylsiloxy)methyl]-4-phenyl-2-oxobicyclo[4.3.0]nonane

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Technology Process of (6R)-1-aza-6-[(tert-butyldimethylsiloxy)methyl]-4-phenyl-2-oxobicyclo[4.3.0]nonane

There total 5 articles about (6R)-1-aza-6-[(tert-butyldimethylsiloxy)methyl]-4-phenyl-2-oxobicyclo[4.3.0]nonane 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:

: 157662-41-4
(R)-(-)-N-(benzyloxycarbonyl)-2-(2'-oxoethyl)proline methyl ester

: 325460-66-0
(6R)-1-aza-6-[(tert-butyldimethylsiloxy)methyl]-4-phenyl-2-oxobicyclo[4.3.0]nonane

Guidance literature:: Multi-step reaction with 6 steps

1: 9.96 g / CH₂Cl₂ / -78 - 20 °C

2: 61 percent / BF₃*Et₂O / diethyl ether; tetrahydrofuran / -78 - -20 °C

3: H₂ / Pd/BaSO₄ / methanol

4: 2.4 g / Et₃N / toluene / 21 h / Heating

5: 93 percent / LiBH₄ / tetrahydrofuran / 0 - 20 °C

6: 96 percent / 2,6-lutidine / CH₂Cl₂ / 1 h / 0 °C

With 2,6-dimethylpyridine; lithium borohydride; boron trifluoride diethyl etherate; hydrogen; triethylamine; Pd-BaSO₄; In tetrahydrofuran; methanol; diethyl ether; dichloromethane; toluene; 1: Wittig reaction / 2: Addition / 3: Hydrogenolysis / 4: cyclocondensation / 5: Reduction / 6: Condensation;
DOI:10.1016/S0040-4020(00)00886-3

Reference yield:

: 325460-62-6
(2R)-N-(benzyloxycarbonyl)-2-[(E)-3'-(carbomethoxy)prop-2'-enyl]proline methyl ester

: 325460-66-0
(6R)-1-aza-6-[(tert-butyldimethylsiloxy)methyl]-4-phenyl-2-oxobicyclo[4.3.0]nonane

Guidance literature:: Multi-step reaction with 5 steps

1: 61 percent / BF₃*Et₂O / diethyl ether; tetrahydrofuran / -78 - -20 °C

2: H₂ / Pd/BaSO₄ / methanol

3: 2.4 g / Et₃N / toluene / 21 h / Heating

4: 93 percent / LiBH₄ / tetrahydrofuran / 0 - 20 °C

5: 96 percent / 2,6-lutidine / CH₂Cl₂ / 1 h / 0 °C

With 2,6-dimethylpyridine; lithium borohydride; boron trifluoride diethyl etherate; hydrogen; triethylamine; Pd-BaSO₄; In tetrahydrofuran; methanol; diethyl ether; dichloromethane; toluene; 1: Addition / 2: Hydrogenolysis / 3: cyclocondensation / 4: Reduction / 5: Condensation;
DOI:10.1016/S0040-4020(00)00886-3

Reference yield:

: 325460-63-7
(2R)-N-(benzyloxycarbonyl)-2-[2'-(phenyl)-3'-(carbomethoxy)-propyl]proline methyl ester

: 325460-66-0
(6R)-1-aza-6-[(tert-butyldimethylsiloxy)methyl]-4-phenyl-2-oxobicyclo[4.3.0]nonane

Guidance literature:: Multi-step reaction with 4 steps

1: H₂ / Pd/BaSO₄ / methanol

2: 2.4 g / Et₃N / toluene / 21 h / Heating

3: 93 percent / LiBH₄ / tetrahydrofuran / 0 - 20 °C

4: 96 percent / 2,6-lutidine / CH₂Cl₂ / 1 h / 0 °C

With 2,6-dimethylpyridine; lithium borohydride; hydrogen; triethylamine; Pd-BaSO₄; In tetrahydrofuran; methanol; dichloromethane; toluene; 1: Hydrogenolysis / 2: cyclocondensation / 3: Reduction / 4: Condensation;
DOI:10.1016/S0040-4020(00)00886-3