Reaktion #44052

ord-035b29cea70c4784b09c078f19050a49

Reaktionsgleichung

CC(=O)c1cccc(Br)c1
1-(3-bromophenyl)ethanone
O=C1CCCN1
2-pyrrolidinone
→
CC(=O)c1cccc(N2CCCC2=O)c1
title compound
Ausbeute 98.0%
CC(=O)c1cccc(N2CCCC2=O)c1
1-(3-Acetylphenyl)-2-pyrrolidinone
Ausbeute 98.0%

Edukte

CC(=O)c1cccc(Br)c1
1-(3-bromophenyl)ethanone
—
amides
—
ureas
—
carbamates
O=C1CCCN1
2-pyrrolidinone

Reagenzien

Keine

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Vorschrift

The title compound was prepared in 98% yield according to the general procedure for the preparation of the amides, ureas and carbamates (Method A) starting from 1-(3-bromophenyl)ethanone and 2-pyrrolidinone.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07732600B2uspto-grants-2010_06