Ethyl 2-(2-ethoxy-2-oxoethyl)-2-methyl-1,3-thiazolidine-3-carboxylate

Base Information

• Chemical Name: Ethyl 2-(2-ethoxy-2-oxoethyl)-2-methyl-1,3-thiazolidine-3-carboxylate
• CAS No.: 41205-37-2
• Molecular Formula: C11H19NO4S
• Molecular Weight: 261.3379
• NSC Number: 345848
• DSSTox Substance ID: DTXSID201203774

Synonyms:41205-37-2;NSC345848;NSC 345848;Ethyl 2-(2-ethoxy-2-oxoethyl)-2-methyl-1,3-thiazolidine-3-carboxylate;2-Thiazolidineacetic acid, 3-(ethoxycarbonyl)2-methyl-, ethyl ester;DTXSID201203774;NSC-345848;Ethyl 3-(ethoxycarbonyl)-2-methyl-2-thiazolidineacetate;ethyl 2-(2-ethoxy-2-oxo-ethyl)-2-methyl-thiazolidine-3-carboxylate

Chemical Property of Ethyl 2-(2-ethoxy-2-oxoethyl)-2-methyl-1,3-thiazolidine-3-carboxylate

Chemical Property:

• Vapor Pressure: 6.67E-05mmHg at 25°C
• Boiling Point: 344.2°C at 760 mmHg
• Flash Point: 162°C
• Density: 1.157g/cm³
• XLogP3: 1.5
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 6
• Exact Mass: 261.10347926
• Heavy Atom Count: 17
• Complexity: 297

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCOC(=O)CC1(N(CCS1)C(=O)OCC)C

Technology Process of Ethyl 2-(2-ethoxy-2-oxoethyl)-2-methyl-1,3-thiazolidine-3-carboxylate

There total 2 articles about Ethyl 2-(2-ethoxy-2-oxoethyl)-2-methyl-1,3-thiazolidine-3-carboxylate 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:

ethyl acetoacetate (141-97-9) → 2-ethoxycarbonylmethyl-2-methyl-thiazolidine-3-carboxylic acid ethyl ester (41205-37-2)

Guidance literature:

Multi-step reaction with 2 steps

1: 24 h / 60 - 70 °C

2: diethyl ether

In diethyl ether;

DOI:10.1021/jm00262a023

Reference yield:

chloroformic acid ethyl ester (541-41-3) + (2-methyl-thiazolidin-2-yl)-acetic acid ethyl ester (770-78-5) → 2-ethoxycarbonylmethyl-2-methyl-thiazolidine-3-carboxylic acid ethyl ester (41205-37-2)

Guidance literature:

In diethyl ether;

DOI:10.1021/jm00262a023

upstream raw materials:

chloroformic acid ethyl ester

(2-methyl-thiazolidin-2-yl)-acetic acid ethyl ester

ethyl acetoacetate

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