(R)-2-[(1R,2S,3S,4R)-2-Formyl-4-methyl-3-(3-oxo-butyl)-cyclohexyl]-propionic acid methyl ester

Base Information

Chemical Name:(R)-2-[(1R,2S,3S,4R)-2-Formyl-4-methyl-3-(3-oxo-butyl)-cyclohexyl]-propionic acid methyl ester
CAS No.:103775-34-4
Molecular Formula:C₁₆H₂₆O₄
Molecular Weight:282.38
Hs Code.:

Synonyms:(R)-2-[(1R,2S,3S,4R)-2-Formyl-4-methyl-3-(3-oxo-butyl)-cyclohexyl]-propionic acid methyl ester

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Chemical Property of (R)-2-[(1R,2S,3S,4R)-2-Formyl-4-methyl-3-(3-oxo-butyl)-cyclohexyl]-propionic acid methyl ester

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Technology Process of (R)-2-[(1R,2S,3S,4R)-2-Formyl-4-methyl-3-(3-oxo-butyl)-cyclohexyl]-propionic acid methyl ester

There total 18 articles about (R)-2-[(1R,2S,3S,4R)-2-Formyl-4-methyl-3-(3-oxo-butyl)-cyclohexyl]-propionic acid methyl ester 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:

: 85031-63-6
5α-hydroperoxy-amorph-5-en-12-oic acid methyl ester

: 103775-34-4
(R)-2-[(1R,2S,3S,4R)-2-Formyl-4-methyl-3-(3-oxo-butyl)-cyclohexyl]-propionic acid methyl ester

: 63968-64-9
C₁₂H₁₃O₂(CH₃)3(O)(OO)

Guidance literature:: 5α-hydroperoxy-amorph-5-en-12-oic acid methyl ester; With trifluoroacetic acid; In chloroform-d1; at -40.15 ℃;

With oxygen; In chloroform-d1; at -0.15 ℃; for 1.66667h;
DOI:10.1016/S0040-4020(01)01192-9

Reference yield:

: 87391-99-9
2-(4,7-dimethyl-(1α-H),2,3,(4β-H),(4aα-H),5,6,(8aα-H)-octahydronaphthalen-1-yl)propionic acid methyl ester

: 103775-34-4
(R)-2-[(1R,2S,3S,4R)-2-Formyl-4-methyl-3-(3-oxo-butyl)-cyclohexyl]-propionic acid methyl ester

Guidance literature:: With dimethylsulfide; ozone; Multistep reaction; 1.) CH₃OH, CH₂Cl₂, -78 deg C, 2.) RT, 2 h;
DOI:10.1016/S0040-4020(01)87487-1