Functionalized fluorinated arylethers by ring-opening of 1,2,3,4-tetrafluorodibenz[b,f][1,4]oxazepine |
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Authors: | Brenda Doherty M.Shane Sloan |
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Affiliation: | School of Chemistry, Queen’s University Belfast, David Keir Building, Belfast BT9 5AG, UK |
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Abstract: | Treatment of 1,2,3,4-tetrafluorodibenz[b,f][1,4]oxazepine with acetyl or benzoyl chloride produces the fluorinated aryl ethers bearing amide and aldehyde functionalities, RCONHC6H4-2-OC6F4CHO-2 (2a R=Ph; 2b R=Me). The structures of intermediate compounds produced by addition of acid chloride across the imine bond and by partial hydrolyis of the resulting chlorine-containing compound have been determined. |
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Keywords: | Dibenzoxazepine Arylethers Crystal structure Ring-opening |
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