methyl 1-((tert-butoxycarbonylamino)(p-tolyl)methyl)-2-oxocyclohexanecarboxylate

Base Information

Chemical Name:methyl 1-((tert-butoxycarbonylamino)(p-tolyl)methyl)-2-oxocyclohexanecarboxylate
CAS No.:1242246-31-6
Molecular Formula:C₂₁H₂₉NO₅
Molecular Weight:375.465
Hs Code.:

Synonyms:methyl 1-((tert-butoxycarbonylamino)(p-tolyl)methyl)-2-oxocyclohexanecarboxylate

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Chemical Property of methyl 1-((tert-butoxycarbonylamino)(p-tolyl)methyl)-2-oxocyclohexanecarboxylate

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Technology Process of methyl 1-((tert-butoxycarbonylamino)(p-tolyl)methyl)-2-oxocyclohexanecarboxylate

There total 2 articles about methyl 1-((tert-butoxycarbonylamino)(p-tolyl)methyl)-2-oxocyclohexanecarboxylate 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:

: 41302-34-5
2-(methoxycarbonyl)cyclohexanone

: 479423-39-7
4-methylbenzaldehyde N-(tert-butoxycarbonyl)imine

: 1203706-54-0
(S)-methyl 1-((R)-(tert-butoxycarbonylamino)(p-tolyl)methyl)-2-oxocyclohexanecarboxylate

: 1242246-31-6
methyl 1-((tert-butoxycarbonylamino)(p-tolyl)methyl)-2-oxocyclohexanecarboxylate

Guidance literature:: With n-butyllithium; (R)-3,3′-bis(3,4,5-trifluorophenyl)[1,1′-binaphthalene]-2,2′-diol; tert-butyl alcohol; In hexane; toluene; at -78 ℃; for 2h; optical yield given as %ee; enantioselective reaction; Inert atmosphere;
DOI:10.1021/ja909874b

Reference yield:

: 41302-34-5
2-(methoxycarbonyl)cyclohexanone

: 479423-39-7
4-methylbenzaldehyde N-(tert-butoxycarbonyl)imine

: 1203706-54-0
(S)-methyl 1-((R)-(tert-butoxycarbonylamino)(p-tolyl)methyl)-2-oxocyclohexanecarboxylate

: 1242246-31-6
C₂₁H₂₉NO₅

Guidance literature:: With n-butyllithium; (R)-3,3′-bis(3,4,5-trifluorophenyl)[1,1′-binaphthalene]-2,2′-diol; tert-butyl alcohol; In hexane; toluene; at -78 ℃; for 2h; optical yield given as %ee; enantioselective reaction; Inert atmosphere;
DOI:10.1055/s-0030-1258296