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Citation
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HERO ID
2849943
Reference Type
Journal Article
Title
The carbomethylation of arylacrylamides leading to 3-ethyl-3-substituted indolin-2-one by cascade radical addition/cyclization
Author(s)
Dai, Q; Yu, J; Jiang, Y; Guo, S; Yang, H; Cheng, J
Year
2014
Is Peer Reviewed?
Yes
Journal
Chemical Communications
ISSN:
1359-7345
EISSN:
1364-548X
Volume
50
Issue
29
Page Numbers
3865-3867
Language
English
PMID
24589915
DOI
10.1039/c4cc01053a
Abstract
An FeCl2-promoted carbomethylation of arylacrylamides by di-tert-butyl peroxide (DTBP) is achieved, leading to 3-ethyl-3-substituted indolin-2-one in high yield. The reaction tolerates a series of functional groups, such as cyano, nitro, ethyloxy carbonyl, bromo, chloro, and trifluoromethyl groups. The radical methylation and arylation of the alkenyl group are involved in this reaction.
Tags
IRIS
•
ETBE
Combined Dataset (After duplicates removed electronically)
Excluded / Not on Topic
Other chemical/non ETBE studies
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