1H-Pyrrole-2-carboxylic acid, 5-[[5-[(1,1-dimethylethoxy)carbonyl]-3-methyl-4-(2-methylpropyl)-1H-pyrr ol-2-yl]methyl]-4-ethyl-3-methyl-, phenylmethyl ester

Base Information

Chemical Name:1H-Pyrrole-2-carboxylic acid, 5-[[5-[(1,1-dimethylethoxy)carbonyl]-3-methyl-4-(2-methylpropyl)-1H-pyrr ol-2-yl]methyl]-4-ethyl-3-methyl-, phenylmethyl ester
CAS No.:143257-25-4
Molecular Formula:C₃₀H₄₀N₂O₄
Molecular Weight:492.659
Hs Code.:
Mol file:143257-25-4.mol

1H-Pyrrole-2-carboxylic acid,
5-[[5-[(1,1-dimethylethoxy)carbonyl]-3-methyl-4-(2-methylpropyl)-1H-pyrr
ol-2-yl]methyl]-4-ethyl-3-methyl-, phenylmethyl ester

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Chemical Property of 1H-Pyrrole-2-carboxylic acid, 5-[[5-[(1,1-dimethylethoxy)carbonyl]-3-methyl-4-(2-methylpropyl)-1H-pyrr ol-2-yl]methyl]-4-ethyl-3-methyl-, phenylmethyl ester

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Technology Process of 1H-Pyrrole-2-carboxylic acid, 5-[[5-[(1,1-dimethylethoxy)carbonyl]-3-methyl-4-(2-methylpropyl)-1H-pyrr ol-2-yl]methyl]-4-ethyl-3-methyl-, phenylmethyl ester

There total 3 articles about 1H-Pyrrole-2-carboxylic acid, 5-[[5-[(1,1-dimethylethoxy)carbonyl]-3-methyl-4-(2-methylpropyl)-1H-pyrr ol-2-yl]methyl]-4-ethyl-3-methyl-, phenylmethyl 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: 64.0%

: 3750-36-5
benzyl 5-(acetoxymethyl)-4-ethyl-3-methyl-1H-pyrrole-2-carboxylate

: 143257-24-3
3-Isobutyl-4-methyl-1H-pyrrole-2-carboxylic acid tert-butyl ester

: 143257-25-4
C₃₀H₄₀N₂O₄

Guidance literature:: With K-10 montmorillonite;
DOI:10.1016/S0040-4020(01)90123-1

Reference yield:

: 2769-72-4
tert-Butyl isocyanoacetate

: 143257-25-4
C₃₀H₄₀N₂O₄

Guidance literature:: Multi-step reaction with 2 steps

1: 54 percent

2: 64 percent / K-10 montmorillonite

With K-10 montmorillonite;
DOI:10.1016/S0040-4020(01)90123-1

Reference yield:

: 143257-35-6
2-nitro-3-acetoxy-5-methylhexane

: 143257-25-4
C₃₀H₄₀N₂O₄

Guidance literature:: Multi-step reaction with 2 steps

1: 54 percent

2: 64 percent / K-10 montmorillonite

With K-10 montmorillonite;
DOI:10.1016/S0040-4020(01)90123-1