(1R)-2-cyclohexylmethylaminocarbonyl-2-cyclopentene-1-carboxylic acid methyl ester

Base Information

Chemical Name:(1R)-2-cyclohexylmethylaminocarbonyl-2-cyclopentene-1-carboxylic acid methyl ester
CAS No.:277751-32-3
Molecular Formula:C₁₅H₂₃NO₃
Molecular Weight:265.353
Hs Code.:

Synonyms:(1R)-2-cyclohexylmethylaminocarbonyl-2-cyclopentene-1-carboxylic acid methyl ester

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Chemical Property of (1R)-2-cyclohexylmethylaminocarbonyl-2-cyclopentene-1-carboxylic acid methyl ester

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Technology Process of (1R)-2-cyclohexylmethylaminocarbonyl-2-cyclopentene-1-carboxylic acid methyl ester

There total 5 articles about (1R)-2-cyclohexylmethylaminocarbonyl-2-cyclopentene-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: 51.0%

: 3218-02-8
cyclohexylmethylamine

: 277751-25-4
(+)-cyclopentyl-2-ene-1,2-dicarboxylic acid 1-methyl ester

: 277751-32-3
(1R)-2-cyclohexylmethylaminocarbonyl-2-cyclopentene-1-carboxylic acid methyl ester

Guidance literature:: With bis-(2-oxo-3-oxazolidinyl)phosphoryl chloride; triethylamine; In N,N-dimethyl-formamide; at 0 - 20 ℃; pH=8;
DOI:10.1021/jm990557t

Reference yield:

: 5307-99-3
(+/-)-7,7-dichlorobicyclo[3.2.0]hept-2-en-6-one

: 277751-32-3
(1R)-2-cyclohexylmethylaminocarbonyl-2-cyclopentene-1-carboxylic acid methyl ester

Guidance literature:: Multi-step reaction with 4 steps

1.1: aq. NaHCO₃ / 5 h / 75 °C

2.1: 97 percent / p-toluenesulfonic acid monohydrate

3.1: NaClO₂; resorcinol; NaH₂PO₄*H₂O / 2-methyl-propan-2-ol; H₂O / 5 h

3.2: via salt with (-)-ephedrine

4.1: 51 percent / bis(2-oxo-3-oxazolidinylphosphinic chloride; Et₃N / dimethylformamide / 0 - 20 °C / pH 8

With sodium chlorite; sodium dihydrogenphosphate; bis-(2-oxo-3-oxazolidinyl)phosphoryl chloride; sodium hydrogencarbonate; toluene-4-sulfonic acid; triethylamine; recorcinol; In water; N,N-dimethyl-formamide; tert-butyl alcohol; 1.1: Hydrolysis / 2.1: Esterification / 3.1: Oxidation / 3.2: Optical resolution / 4.1: Condensation;
DOI:10.1021/jm990557t

Reference yield:

: 30758-76-0
(+/-)-2-formylcyclopent-2-enecarboxylic acid

: 277751-32-3
(1R)-2-cyclohexylmethylaminocarbonyl-2-cyclopentene-1-carboxylic acid methyl ester

Guidance literature:: Multi-step reaction with 3 steps

1.1: 97 percent / p-toluenesulfonic acid monohydrate

2.1: NaClO₂; resorcinol; NaH₂PO₄*H₂O / 2-methyl-propan-2-ol; H₂O / 5 h

2.2: via salt with (-)-ephedrine

3.1: 51 percent / bis(2-oxo-3-oxazolidinylphosphinic chloride; Et₃N / dimethylformamide / 0 - 20 °C / pH 8

With sodium chlorite; sodium dihydrogenphosphate; bis-(2-oxo-3-oxazolidinyl)phosphoryl chloride; toluene-4-sulfonic acid; triethylamine; recorcinol; In water; N,N-dimethyl-formamide; tert-butyl alcohol; 1.1: Esterification / 2.1: Oxidation / 2.2: Optical resolution / 3.1: Condensation;
DOI:10.1021/jm990557t