(2R,1'R)-ethyl 2-(p-methoxyphenylamino)-2-(2'-oxocyclohex-1'-yl)-acetate

Base Information

Chemical Name:(2R,1'R)-ethyl 2-(p-methoxyphenylamino)-2-(2'-oxocyclohex-1'-yl)-acetate
CAS No.:409113-12-8
Molecular Formula:C₁₇H₂₃NO₄
Molecular Weight:305.374
Hs Code.:

Synonyms:(2R,1'R)-ethyl 2-(p-methoxyphenylamino)-2-(2'-oxocyclohex-1'-yl)-acetate

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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 (2R,1'R)-ethyl 2-(p-methoxyphenylamino)-2-(2'-oxocyclohex-1'-yl)-acetate

Chemical Property:

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Technology Process of (2R,1'R)-ethyl 2-(p-methoxyphenylamino)-2-(2'-oxocyclohex-1'-yl)-acetate

There total 11 articles about (2R,1'R)-ethyl 2-(p-methoxyphenylamino)-2-(2'-oxocyclohex-1'-yl)-acetate 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: 45.0%

: 108-94-1,11119-77-0,9003-41-2,9075-99-4
cyclohexanone

: 115276-75-0,124156-21-4,120419-96-7
ethyl (E)-2-(p-methoxyphenylimino)acetate

: 409113-12-8
(2R,1'R)-ethyl 2-(p-methoxyphenylamino)-2-(2'-oxocyclohex-1'-yl)-acetate

Guidance literature:: L-proline; In water; dimethyl sulfoxide; at 20 ℃; for 18h;
DOI:10.1002/adsc.200700110

Reference yield:

: 124156-21-4
ethyl (4-methoxyphenylimino)acetate

: 108-94-1,11119-77-0,9003-41-2,9075-99-4
cyclohexanone

: ethyl 2-(p-methoxyphenylamino)-2-(2’-oxocyclohexyl)acetate

: 409113-12-8
(2R,1'R)-ethyl 2-(p-methoxyphenylamino)-2-(2'-oxocyclohex-1'-yl)-acetate

: 409113-04-8
ethyl (S)-2-(4-methoxyphenylamino)-2-((S)-2-oxocyclohexyl)-acetate

Guidance literature:: With O-lauroyl-trans-4-hydroxy-L-proline; sodium hydrogencarbonate; In water; at 20 ℃; for 24h; Reagent/catalyst; Overall yield = 49 %;
DOI:10.1016/j.tetasy.2013.03.016