Abstract Described are processes for preparing novel 4- and 5-phenyl-pentenals, lower alkyl and lower alkylene acetals thereof having the structure: ##STR1## wherein one of X and Y is phenyl and the other of X and Y is hydrogen and A is a moiety selected from the group consisting of: ##STR2## WHEREIN R b and R b ' separately are the same or different lower alkyl or R b and R b ' taken together form a lower alkylene group either (i) comprising the step of intimately admixing the lithium salt of a Schiff base of acetaldehyde and an amine with a phenyl-substituted compound selected from the group consisting of phenyl alkanals and phenyl alkenyl bromides in order to produce a phenyl-substituted Schiff base and treating said phenyl-substituted Schiff base with an acid, or (ii) comprising the steps of first admixing phenyl propionaldehyde with a tri-substituted formyl methylene phosphorane in a non-reactive solvent and then heating the resulting mixture.
The process of preparing a phenyl pentenal selected from the group consisting of 5-phenyl-4-pentenal and 4-phenyl-4-pentenal comprising the steps of (i) reacting a phenyl alkenyl bromide selected from the group consisting of phenyl allyl bromide having the structure: ##STR26## and α-bromomethyl styrene having the structure: ##STR27## with the lithium salt of a Schiff base of acetaldehyde with an organic amine thereby forming a 4- or 5-phenyl-4-pentenal Schiff base, the temperature range of the reaction between the phenyl alkenyl bromide and the Schiff base being from -70° C. up to +30° C., and (ii) subsequently acidifying the resultant 4- or 5-phenyl-4-pentenal Schiff base at a pH of approximately 1 with an acid selected from the group consisting of hydrochloric acid and sulfuric acid.
Claim 2
Dependent Claim
122 words
The process of preparing a phenyl pentenal selected from the group consisting of 5-phenyl-4-pentenal and 4-phenyl-4-pentenal comprising the steps of (i) reacting a phenyl alkenyl bromide selected from the group consisting of phenyl allyl bromide having the structure: ##STR26## and α-bromomethyl styrene having the structure: ##STR27## with the lithium salt of a Schiff base of acetaldehyde with an organic amine thereby forming a 4- or 5-phenyl-4-pentenal Schiff base, the temperature range of the reaction between the phenyl alkenyl bromide and the Schiff base being from -70° C. up to +30° C., and (ii) subsequently acidifying the resultant 4- or 5-phenyl-4-pentenal Schiff base at a pH of approximately 1 with an acid selected from the group consisting of hydrochloric acid and sulfuric acid.