Reaktion #355536

ord-6ac70b13ca7c46c8b412452945197134

Reaktionsgleichung

Clc1ccc2oc(-c3ccccc3)cc2c1
5 -chloro-2-phenylbenzofuran
CCN(CC)CCOc1ccccc1C(=O)Cl.Cl
2-(2-diethylaminoethoxy)benzoyl chloride hydrochloride
→
CCN(CC)CCOc1ccccc1C(=O)c1c(-c2ccccc2)oc2ccc(Cl)cc12
title compound
CCN(CC)CCOc1ccccc1C(=O)c1c(-c2ccccc2)oc2ccc(Cl)cc12
5-Chloro-3-[2-(2-diethylaminoethoxy)benzoyl]-2-phenylbenzofuran

Edukte

Clc1ccc2oc(-c3ccccc3)cc2c1
5 -chloro-2-phenylbenzofuran
CCN(CC)CCOc1ccccc1C(=O)Cl.Cl
2-(2-diethylaminoethoxy)benzoyl chloride hydrochloride

Reagenzien

Keine

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Vorschrift

Acylation of 5 -chloro-2-phenylbenzofuran with 2-(2-diethylaminoethoxy)benzoyl chloride hydrochloride by the procedure described in Example 6 gives the title compound.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US03947470uspto-grants-1976_03