Butanoic acid, 4-amino-, 1-methylethyl ester

Base Information

• Chemical Name: Butanoic acid, 4-amino-, 1-methylethyl ester
• CAS No.: 17088-67-4
• Molecular Formula: C7H15NO2
• Molecular Weight: 145.202
• Mol file: 17088-67-4.mol

Synonyms:Isopropyl-γ-aminobutyrat;

Chemical Property of Butanoic acid, 4-amino-, 1-methylethyl ester

Chemical Property:

• PSA: 52.32000
• LogP: 1.37720

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

Technology Process of Butanoic acid, 4-amino-, 1-methylethyl ester

There total 1 articles about Butanoic acid, 4-amino-, 1-methylethyl 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:

isopropyl alcohol (67-63-0,8013-70-5) + 4-amino-n-butyric acid (56-12-2) → isopropyl γ-aminobutyrate (17088-67-4)

Guidance literature:

Multistep reaction; (i) SOCl₂, CH₂Cl₂, (ii) /BRN= 635639/;

Reference yield:

isopropyl γ-aminobutyrate (17088-67-4) → 2-pyrrolidinon (616-45-5)

Guidance literature:

In tert-Amyl alcohol; at 40 ℃; for 72h; porcine pancreatic lipase or subtilisin;

DOI:10.1016/S0040-4039(00)74825-8

Reference yield:

isopropyl γ-aminobutyrate (17088-67-4) + O-acetylsalicyloyl chloride (5538-51-2) → C14H19NO4

Guidance literature:

With sodium hydrogencarbonate; triethylamine; In dichloromethane; for 18h; Reflux;

DOI:10.1248/cpb.c14-00329

upstream raw materials:

isopropyl alcohol

4-amino-n-butyric acid

Downstream raw materials:

2-pyrrolidinon

Refernces