19352-94-4

Basic information

• Product Name: 3-Buten-2-one, 4-(1-pyrrolidinyl)- (8CI,9CI)
• Synonyms: 3-Buten-2-one, 4-(1-pyrrolidinyl)- (8CI,9CI)
• CAS NO: 19352-94-4
• Molecular Formula: C₈H₁₃NO
• Molecular Weight: 139.19492
• Product Categories: ACETYLGROUP
• Mol File: 19352-94-4.mol
• Article Data: 8

Chemical Properties

• Appearance: /
• Refractive Index: 1.57
• CAS DataBase Reference: 3-Buten-2-one, 4-(1-pyrrolidinyl)- (8CI,9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Buten-2-one, 4-(1-pyrrolidinyl)- (8CI,9CI)(19352-94-4)
• EPA Substance Registry System: 3-Buten-2-one, 4-(1-pyrrolidinyl)- (8CI,9CI)(19352-94-4)

Safety Data

• Hazardous Substances Data: 19352-94-4(Hazardous Substances Data)

Usage

InChI:InChI=1/C8H13NO/c1-8(10)4-7-9-5-2-3-6-9/h4,7H,2-3,5-6H2,1H3

Upstream product

• 123-75-1 pyrrolidine 
• 87419-51-0 3-Oxo-2,3-dihydrothiophene 1,1-dioxide 
• 4652-27-1 4-methoxy-3-buten-2-one 
• 51731-17-0 trans-4-methoxy-3-buten-2-one 
• 23074-57-9 4-ethoxybut-3-en-2-one 
• 14716-77-9 1-(1-imidazolyl)-1-buten-3-one 
• 91860-01-4 1-(3-oxo-1-buten-1-yl)-3-methylimidazolium iodide 
• 41125-09-1 3-oxo-butyraldehyde; sodium enolate 

Downstream Products

• 1367352-54-2 C₁₆H₂₆N₂O 
• 87005-15-0 α-bromoacetoacetaldehyde 
• 223761-49-7 4-(Pyrrolidin-1-yl)but-3-in-2-on 

Relevant articles and documents

A Method for the Preparation of β-Amino-α,β-unsaturated Carbonyl Compounds: Study of Solvent Effect and Mechanism

An efficient method for the preparation of β-amino-α,β-unsaturated carbonyl compounds is demonstrated. Bench-stable sodium 3-oxo-enolates were prepared from carbonyl compounds, and reacted with amines in the presence of an acid and a desiccant. DFT studie

1-amino-3-siloxy-1,3-butadienes: Highly reactive dienes for the Diels- Alder reaction

1-Amino-3-siloxy-1,3-butadienes represent a novel class of heteroatom- containing dienes with several useful properties. These dienes can be prepared efficiently by deprotonation of readily available vinylogous amides with potassium hexamethylsilazide, followed by silylation of the corresponding potassium enolates. This protocol has been found to be quite general for the preparation of various dienes containing different silyl and amino groups. Amino siloxy dienes readily undergo [4 + 2] cycloadditions with a wide range of electron-deficient dienophiles. The reactions generally occur under very mild conditions to afford the corresponding [4 + 2] adducts in high yields and with complete regioselectivity. High endo selectivity is observed in the case of N-phenylmaleimide and methacrolein. Other cycloadducts are usually obtained as mixtures of endo/exo diastereomers. The cycloadducts are versatile synthetic intermediates. They can be subjected to deprotonation, reduction, and Wittig olefination without any hydrolysis or elimination. In addition, the elimination of the amino group can be cleanly accomplished under acidic conditions leading to the formation of enones. A variety of substituted cyclohexenones can be prepared by this procedure.

Additions of nucleophiles to 3-oxo-2,3-dihydrothiophene 1,1-dioxides. Formation of vinyl sulfides, thioacetals and enaminones

3-Oxo-2,3-dihydrothiophene 1,1-dioxide (la) was prepared by oxidation of the commercially available 3methoxythiophene with dimethyldioxirane. Some other substituted 3-methoxythiophene derivatives were oxidized as well. Although the yields of these reactio