1,4,4-Trimethyl-2-oxopyrrolidin-3-yl prop-2-enoate

Base Information

Chemical Name:1,4,4-Trimethyl-2-oxopyrrolidin-3-yl prop-2-enoate
CAS No.:737762-15-1
Molecular Formula:C₁₀H₁₅NO₃
Molecular Weight:197.234
Hs Code.:
DSSTox Substance ID:DTXSID90461585
Nikkaji Number:J2.126.807K
Mol file:737762-15-1.mol

Synonyms:737762-15-1;1,4,4-Trimethyl-2-oxopyrrolidin-3-yl prop-2-enoate;DTXSID90461585

Suppliers and Price of 1,4,4-Trimethyl-2-oxopyrrolidin-3-yl prop-2-enoate

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
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price

Total 1 raw suppliers

Chemical Property of 1,4,4-Trimethyl-2-oxopyrrolidin-3-yl prop-2-enoate

Chemical Property:

PSA：46.61000
LogP:0.52030
XLogP3:1.2
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:197.10519334
Heavy Atom Count:14
Complexity:283

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1(CN(C(=O)C1OC(=O)C=C)C)C

Technology Process of 1,4,4-Trimethyl-2-oxopyrrolidin-3-yl prop-2-enoate

There total 2 articles about 1,4,4-Trimethyl-2-oxopyrrolidin-3-yl prop-2-enoate 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: 65.0%

: 89895-63-6
(+/-)-3-hydroxy-1,4,4-trimethyl-2-pyrrolidinone

: 814-68-6,25189-84-8
acryloyl chloride

: 737762-15-1
(+/-)-1,4,4-trimethyl-2-oxopyrrolin-3-yl acrylate

Guidance literature:: With triethylamine; In dichloromethane; at -20 ℃; for 2h;
DOI:10.1002/ejoc.200400019

Reference yield:

: 79-50-5
pantolactone

: 737762-15-1
(+/-)-1,4,4-trimethyl-2-oxopyrrolin-3-yl acrylate

Guidance literature:: Multi-step reaction with 2 steps

1: 65 percent / triethylamine / CH₂Cl₂ / 2 h / -20 °C

With triethylamine; In dichloromethane;
DOI:10.1002/ejoc.200400019