Published 2008 | Version v1
Journal article

Synthesis of 1-indanones through the intramolecular Friedel-Crafts acylation reaction using NbCl5 as Lewis acid

  • 1. Universidade de Sao Paulo, Ribeirao Preto, SP (Brazil). Faculdade de Filosofia, Ciencias e Letras. Dept. de Quimica

Description

The intramolecular Friedel-Crafts acylation reaction of 3-arylpropanoic acids to give 1-indanones can be effected in good yields under mild conditions (room temperature) by using niobium pentachloride. Our results indicate that NbCl5 acts both as reagent (to transform carboxylic acids into acyl chlorides) and as catalyst in the Friedel-Crafts cyclization. (author)

Availability note (English)

Available from http://www.scielo.br/pdf/qn/v31n4/a10v31n4.pdf

Additional details

Additional titles

Original title (Portuguese)
Sintese de 1-indanones atraves da reacao de acilacao de Friedel-Crafts

Publishing Information

Journal Title
Quimica Nova
Journal Volume
31
Journal Issue
4
Journal Page Range
p. 763-766
ISSN
0100-4042
CODEN
QUNODK

Optional Information

Notes
16 refs., 20 figs., 3 tabs.