Publication Cover
Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 41, 2011 - Issue 5
408
Views
4
CrossRef citations to date
0
Altmetric
Original Articles

Acylation of Aromatic Ethers Using Different Carboxylic Acid Anhydrides as Acylating Agents in the Presence of Nontoxic, Noncorrosive Resin Amberlyst 15 as a Solid Acid Catalyst

&
Pages 754-761 | Received 27 Aug 2009, Published online: 31 Jan 2011
 

Abstract

Friedel–Crafts acylation of aromatic ethers, anisole, 2-methoxynaphthalene, and dimethoxybenzenes with different acid anhydrides is carried out in the presence of an inexpensive and nonhazardous solid acid, Amberlyst 15. The catalyst is reusable, thus making the process environmentally friendly.

ACKNOWLEDGMENT

Financial support by the government of India under the “Technical Education Quality Improvement Programme” (TEQIP) is gratefully acknowledged.

Notes

Note. Reaction conditions: Veratrole (10 mmol), acetic anhydride (10 mmol), 80 °C, solvent EDC (10 mL), time 10 h.

a Wt% with regard to amount of veratrole.

b GC analysis.

Note. Reaction conditions: Aromatic ether (10 mmol), acid anhydride (10 mmol), catalyst: Amberlyst 15, 20 wt% with regard to weight of aromatic ether, 80 °C, solvent EDC (10 mL), time 10 h.

a GC and GC-MS analysis.

Log in via your institution

Log in to Taylor & Francis Online

PDF download + Online access

  • 48 hours access to article PDF & online version
  • Article PDF can be downloaded
  • Article PDF can be printed
USD 61.00 Add to cart

Issue Purchase

  • 30 days online access to complete issue
  • Article PDFs can be downloaded
  • Article PDFs can be printed
USD 422.00 Add to cart

* Local tax will be added as applicable

Related Research

People also read lists articles that other readers of this article have read.

Recommended articles lists articles that we recommend and is powered by our AI driven recommendation engine.

Cited by lists all citing articles based on Crossref citations.
Articles with the Crossref icon will open in a new tab.