(1R,2R,3S)-2-<(1S)-1-(tert-Butoxycarbonyl)ethyl>-3-methylcyclohexane-1-carboxylic acid, methyl ester

Base Information

Chemical Name:(1R,2R,3S)-2-<(1S)-1-(tert-Butoxycarbonyl)ethyl>-3-methylcyclohexane-1-carboxylic acid, methyl ester
CAS No.:142459-41-4
Molecular Formula:C₁₆H₂₈O₄
Molecular Weight:284.396
Hs Code.:

Synonyms:(1R,2R,3S)-2-<(1S)-1-(tert-Butoxycarbonyl)ethyl>-3-methylcyclohexane-1-carboxylic acid, methyl ester

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Chemical Property of (1R,2R,3S)-2-<(1S)-1-(tert-Butoxycarbonyl)ethyl>-3-methylcyclohexane-1-carboxylic acid, methyl ester

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Technology Process of (1R,2R,3S)-2-<(1S)-1-(tert-Butoxycarbonyl)ethyl>-3-methylcyclohexane-1-carboxylic acid, methyl ester

There total 9 articles about (1R,2R,3S)-2-<(1S)-1-(tert-Butoxycarbonyl)ethyl>-3-methylcyclohexane-1-carboxylic 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: 56.0%

: 142459-40-3
(E,E)-(S)-2,4-Dimethyl-2,7-nonadienoic acid, 1-tert-butyl 9-methyl diester

: 142459-51-6
tert-Butyl 9-hydroxy-2,4-dimethyl-2-nonenoate

: 142459-41-4
(1R,2R,3S)-2-<(1S)-1-(tert-Butoxycarbonyl)ethyl>-3-methylcyclohexane-1-carboxylic acid, methyl ester

Guidance literature:: With L-Selectride; In tetrahydrofuran; at -80 - -25 ℃; for 1h;
DOI:10.1021/jo00036a026

Reference yield:

: 56904-86-0
tert-butyl 2-(triphenylphosphoranylidene)propionate

: 142459-41-4
(1R,2R,3S)-2-<(1S)-1-(tert-Butoxycarbonyl)ethyl>-3-methylcyclohexane-1-carboxylic acid, methyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 90 percent / acetonitrile / 2 h / Heating

2: 56 percent / L-Selectride / tetrahydrofuran / 1 h / -80 - -25 °C

With L-Selectride; In tetrahydrofuran; acetonitrile;
DOI:10.1021/jo00036a026

Reference yield:

: 25913-88-6,135006-51-8,142459-21-0
(2S)-2-methyl-5-hexen-1-ol

: 142459-41-4
(1R,2R,3S)-2-<(1S)-1-(tert-Butoxycarbonyl)ethyl>-3-methylcyclohexane-1-carboxylic acid, methyl ester

Guidance literature:: Multi-step reaction with 7 steps

1: 99.5 percent / imidazole / CH₂Cl₂ / 0.67 h / Ambient temperature

2: 73 percent / O₃, Me₂S / methanol; CH₂Cl₂ / 1 h

3: 85 percent / benzene / 1.5 h / Heating

4: 94 percent / 5percent HF / acetonitrile / 3 h / Ambient temperature

5: 1) oxalyl chloride, DMSO, 2) Et₃N / 1) CH₂Cl₂, -60 deg C - -25 deg C, 1 h, 2) -20 deg C - -10 deg C

6: 90 percent / acetonitrile / 2 h / Heating

7: 56 percent / L-Selectride / tetrahydrofuran / 1 h / -80 - -25 °C

With 1H-imidazole; oxalyl dichloride; dimethylsulfide; hydrogen fluoride; L-Selectride; ozone; dimethyl sulfoxide; triethylamine; In tetrahydrofuran; methanol; dichloromethane; acetonitrile; benzene;
DOI:10.1021/jo00036a026