126265-30-3

Basic information

• Product Name: N-ALLYL-2-BROMO-ACETAMIDE
• Synonyms: N-ALLYL-2-BROMO-ACETAMIDE;CHEMBRDG-BB 4023687;N-allyl-2-bromoacetamide(SALTDATA: FREE);2-bromo-N-(prop-2-en-1-yl)acetamide
• CAS NO: 126265-30-3
• Molecular Formula: C₅H₈BrNO
• Molecular Weight: 178.03
• Mol File: 126265-30-3.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 285.274°C at 760 mmHg
• Flash Point: 126.33°C
• Appearance: /
• Density: 1.421g/cm³
• Vapor Pressure: 0.003mmHg at 25°C
• Refractive Index: 1.491
• CAS DataBase Reference: N-ALLYL-2-BROMO-ACETAMIDE(CAS DataBase Reference)
• NIST Chemistry Reference: N-ALLYL-2-BROMO-ACETAMIDE(126265-30-3)
• EPA Substance Registry System: N-ALLYL-2-BROMO-ACETAMIDE(126265-30-3)

Safety Data

• Hazardous Substances Data: 126265-30-3(Hazardous Substances Data)

Usage

InChI:InChI=1/C5H8BrNO/c1-2-3-7-5(8)4-6/h2H,1,3-4H2,(H,7,8)

Upstream product

• 598-21-0 2-Bromoacetyl bromide 
• 107-11-9 1-amino-2-propene 
• 22118-09-8 2-bromoacetyl chloride 

Downstream Products

• 1451076-20-2 (±)-1'-allyl-2-(4-methoxybenzyl)spiro[isoindoline-1,3'-pyrrolidine]-2',3,5'-trione 
• 710355-23-0 N-allyl-2-benzylaminoacetamide 

Relevant articles and documents

A SIMPLE AND EFFICIENT ONE POT SYNTHESIS OF 4-OXO-SPIRO AND THEIR REACTIONS WITH DDQ

The treatment of two equivalents of the anion of 3,4-dihydro-1H-quinoline-2-thione (3) with one equivalet of one of the N-substituted 2-bromoacetamides (4a-d) at room temperature afforded the title compounds in good yields (Scheme 1, Table 1).The reaction of the compounds (6a-d) with DDQ at room temperature and 90 deg C was studied.Mechanistic aspects of the processes are briefly discussed.

Microwave-assisted solvent-free intramolecular 1,3-dipolar cycloaddition reactions leading to hexahydrochromeno[4,3-b]pyrroles: scope and limitations

We report the microwave-assisted solvent-free synthesis of hexahydrochromeno[4,3-b]pyrroles. Intramolecular 1,3-dipolar cycloadditions proceed under these conditions within 15-40 min in 16-84% yields. An influence of the microwave irradiation upon various [3+2] cycloaddition reaction intermediates was studied. Additionally, a scope and limitations of these reactions including an influence of the dipolarophile geometry upon the cycloaddition selectivity and steric demands of the dipole upon its reactivity were also disclosed. These observations led us to postulate a preferable transition state of the reaction. Finally, an influence of the microwave irradiation to the isomerization of activated olefins was also described.

Synthesis of γ-Butyrolactams by the Palladium-Catalyzed Cyclization of N-Allylbromoacetamides

N-Allylbromoacetamides undergo cyclizatlon to give γ-butyrolactams in the presence of palladium catalysts and a base. - Key words: Palladium-catalyzed cyclization; γ-Butyrolactam.