Method for preparing para-phenyl alkynyl benzaldehydes
View Patent ↗The present invention is related to a new synthesis for preparing para-phenyl alkynyl benzaldehyde of general formula (I). The compounds of formula (I) are useful building blocks, in particular in the synthesis of electrically conducting polymers. R is selected from the group consisting of C 1 -C 12 -alkyl, C 1 -C 12 -alkyl aryl, C 1 -C 12 -alkyl heteroaryl, C 2 -C 12 -alkenyl, C 2 C 12 -alkenyl aryl, C 2 -C 12 -alkenyl heteroaryl, C 2 -C 12 -alkynyl, C 2 -C 12 -alkynyl aryl, C 2 -C 12 -alkynyl heteroaryl, C 3 -C 8 -cycloalkylC 1 -C 12 -alkyl-C 3 -C 8 -cycloalkyl, C 1 -C 12 -alkoxy, aryl, heteroaryl, halides.
1. A process for the preparation of compounds of formula (I):
wherein R is C 1 -C 12 -alkyl, C 1 -C 12 -alkyl aryl, C 1 -C 12 -alkyl heteroaryl, C 2 -C 12 -alkenyl, C 2 -C 12 -alkenyl aryl, C 2 -C 12 -alkenyl heteroaryl, C 2 -C 12 -alkynyl, C 2 -C 12 -alkynyl aryl, C 2 -C 12 -alkynyl heteroaryl, C 1 -C 12 -alkyl-C 3 -C 8 -cycloalkyl, C 3 -C 8 -cycloalkyl, C 1 -C 12 -alkoxy, aryl, heteroaryl, or a halide;
said process comprising the steps of:
Step 1: reacting an acyl chloride of formula (III) with an alkyl benzene of formula (IV) to yield the corresponding compound (V):
wherein LG is a leaving group;
Step 2: transforming a compound of formula (V) into compound of formula (VI), using a suitable halogenating agent:
Step 3: subjecting a compound (VI) to an elimination reaction to provide a compound of formula (VII):
Step 4: subjecting a compound of formula (VII) or an activated species thereof with a formylating agent (VIII) for giving the compound (I):
2. The process according to claim 1 , wherein the reaction of step 1 is conducted in the presence of AlCl 3 .
3. The process according to claim 1 , wherein the halogenating agent in step 2 is acetyl chloride.
4. The process according to claim 1 , wherein the reaction of step 3 is performed in presence of a base.
5. The process according to claim 1 , wherein the formylating agent in step 4 is selected from the group consisting of DMF, 1-formyl-piperidine, 1-formyl piperazine, N-methyl-N-(2-pyridyl) formamide, N-methyl formanilide, and Weinreb formamide.
6. The process according to claim 1 , wherein the reaction of step 4 is conducted in the presence of magnesium or butyl lithium.
7. The process according to claim 1 , wherein R is C 1 -C 6 alkyl.
8. The process according to claim 1 , wherein the compound is selected from the group consisting of:
4-(4-methoxy-phenylethynyl)-benzaldehyde;
4-(4-hexyl-phenylethynyl)-benzaldehyde;
4-(4-ethyl-phenylethynyl)-benzaldehyde;
4-(4-chloro-phenylethynyl)-benzaldehyde;
4-(4-butyl-phenylethynyl)-benzaldehyde;
4-p-tolylethynyl-benzaldehyde;
4-(4-propyl-phenylethynyl)-benzaldehyde;
4-(4-cyclohexyl-phenylethynyl)-benzaldehyde;
4-(4-propoxy-phenylethynyl)-benzaldehydel;
4-(4-phenoxy-phenylethynyl)-benzaldehyde; and
4-biphenyl-4-ylethynyl-benzaldehyde.
9. The process according to claim 1 , wherein LG is a halide.
10. The process according to claim 1 , wherein the reaction of step 1 is performed in the presence of FeCl 3 .
11. The process according to claim 1 , wherein the reaction of step 1 is performed at a temperature in a range from room temperature to 50° C. for a period of about 5 hours.
12. The process according to claim 1 , wherein the halogenating agent in step 2 is bromide.
13. The process according to claim 1 , wherein the reaction of step 2 is performed at room temperature for a period of 40 hours.
14. The process according to claim 1 , wherein the reaction of step 3 is performed at a temperature of 80° C. for a period of 20 hours.