(S)-2-(((S)-tert-butoxycarbonylamino)(2-chlorophenyl)methyl)-2-cyanocyclopentanone

Base Information

Chemical Name:(S)-2-(((S)-tert-butoxycarbonylamino)(2-chlorophenyl)methyl)-2-cyanocyclopentanone
CAS No.:1123681-73-1
Molecular Formula:C₁₈H₂₁ClN₂O₃
Molecular Weight:348.829
Hs Code.:

Synonyms:(S)-2-(((S)-tert-butoxycarbonylamino)(2-chlorophenyl)methyl)-2-cyanocyclopentanone

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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 (S)-2-(((S)-tert-butoxycarbonylamino)(2-chlorophenyl)methyl)-2-cyanocyclopentanone

Chemical Property:

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Technology Process of (S)-2-(((S)-tert-butoxycarbonylamino)(2-chlorophenyl)methyl)-2-cyanocyclopentanone

There total 2 articles about (S)-2-(((S)-tert-butoxycarbonylamino)(2-chlorophenyl)methyl)-2-cyanocyclopentanone 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: 99.0%

: 848194-75-2
o-chlorobenzaldehyde N-(tert-butoxycarbonyl)imine

: 2941-29-9,138260-51-2
2-oxocyclopentanecarbonitrile

: 1123681-73-1
(S)-2-(((S)-tert-butoxycarbonylamino)(2-chlorophenyl)methyl)-2-cyanocyclopentanone

Guidance literature:: With erbium triisopropoxide; (S)-N-(2-hydroxyphenyl)-2-(2-hydroxybenzoylamino)-3-methylbutylamide; In diethyl ether; at 0 ℃; for 1h; optical yield given as %ee; enantioselective reaction; Inert atmosphere;
DOI:10.1021/ja900084k

Reference yield:

: 848194-75-2
o-chlorobenzaldehyde N-(tert-butoxycarbonyl)imine

: 2941-29-9,138260-51-2
2-oxocyclopentanecarbonitrile

: 1123681-73-1
(S)-2-(((S)-tert-butoxycarbonylamino)(2-chlorophenyl)methyl)-2-cyanocyclopentanone

: C₁₈H₂₁ClN₂O₃

Guidance literature:: With sodium hydrogencarbonate; In diethyl ether; at 0 ℃; for 1.5h; Reagent/catalyst; enantioselective reaction; Catalytic behavior; Molecular sieve; Flow reactor;
DOI:10.1002/chem.201406402