((1R,2R)-2-{2-[6-(tert-Butyl-dimethyl-silanyloxymethyl)-cyclohexa-1,5-dienyl]-2-methoxymethoxy-ethyl}-2-methyl-cyclohexyl)-acetic acid methyl ester

Base Information

Chemical Name:((1R,2R)-2-{2-[6-(tert-Butyl-dimethyl-silanyloxymethyl)-cyclohexa-1,5-dienyl]-2-methoxymethoxy-ethyl}-2-methyl-cyclohexyl)-acetic acid methyl ester
CAS No.:115562-65-7
Molecular Formula:C₂₇H₄₈O₅Si
Molecular Weight:480.761
Hs Code.:

((1R,2R)-2-{2-[6-(tert-Butyl-dimethyl-silanyloxymethyl)-cyclohexa-1,5-dienyl]-2-methoxymethoxy-ethyl}-2-methyl-cyclohexyl)-acetic acid methyl ester

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Chemical Property of ((1R,2R)-2-{2-[6-(tert-Butyl-dimethyl-silanyloxymethyl)-cyclohexa-1,5-dienyl]-2-methoxymethoxy-ethyl}-2-methyl-cyclohexyl)-acetic acid methyl ester

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Technology Process of ((1R,2R)-2-{2-[6-(tert-Butyl-dimethyl-silanyloxymethyl)-cyclohexa-1,5-dienyl]-2-methoxymethoxy-ethyl}-2-methyl-cyclohexyl)-acetic acid methyl ester

There total 5 articles about ((1R,2R)-2-{2-[6-(tert-Butyl-dimethyl-silanyloxymethyl)-cyclohexa-1,5-dienyl]-2-methoxymethoxy-ethyl}-2-methyl-cyclohexyl)-acetic 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: 96.0%

: 107-30-2
chloromethyl methyl ether

: 115562-75-9,115649-69-9
((1R,2R)-2-{2-[6-(tert-Butyl-dimethyl-silanyloxymethyl)-cyclohexa-1,5-dienyl]-2-hydroxy-ethyl}-2-methyl-cyclohexyl)-acetic acid methyl ester

: 115562-65-7,115649-65-5
((1R,2R)-2-{2-[6-(tert-Butyl-dimethyl-silanyloxymethyl)-cyclohexa-1,5-dienyl]-2-methoxymethoxy-ethyl}-2-methyl-cyclohexyl)-acetic acid methyl ester

Guidance literature:: With dmap; N-ethyl-N,N-diisopropylamine; In dichloromethane; for 2h;
DOI:10.1021/jo00252a059

Reference yield:

: 938-07-8
trans-10-methyldecal-2-one

: 115562-65-7,115649-65-5
((1R,2R)-2-{2-[6-(tert-Butyl-dimethyl-silanyloxymethyl)-cyclohexa-1,5-dienyl]-2-methoxymethoxy-ethyl}-2-methyl-cyclohexyl)-acetic acid methyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 1.) p-TsOH, 2.) O₃, NaHCO₃ / 1.) from 25 to 140 deg C, 2.) CH₂Cl₂, MeOH

2: 1.) t-BuLi / 1.) THF, from -78 to -10 deg C

3: 84 percent / NEt₃, DMAP / CH₂Cl₂ / 2 h

4: 96 percent / EtN(i-Pr)2, DMAP / CH₂Cl₂ / 2 h

With dmap; tert.-butyl lithium; sodium hydrogencarbonate; toluene-4-sulfonic acid; ozone; triethylamine; N-ethyl-N,N-diisopropylamine; In dichloromethane;
DOI:10.1021/jo00252a059

Reference yield:

: 115562-63-5
[(1S,2S)-2-Methyl-2-(2-oxo-ethyl)-cyclohexyl]-acetic acid methyl ester

: 115562-65-7,115649-65-5
((1R,2R)-2-{2-[6-(tert-Butyl-dimethyl-silanyloxymethyl)-cyclohexa-1,5-dienyl]-2-methoxymethoxy-ethyl}-2-methyl-cyclohexyl)-acetic acid methyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 1.) t-BuLi / 1.) THF, from -78 to -10 deg C

2: 84 percent / NEt₃, DMAP / CH₂Cl₂ / 2 h

3: 96 percent / EtN(i-Pr)2, DMAP / CH₂Cl₂ / 2 h

With dmap; tert.-butyl lithium; triethylamine; N-ethyl-N,N-diisopropylamine; In dichloromethane;
DOI:10.1021/jo00252a059