Process for preparing 2-acetonaphthones

Claim 2

A process for preparing a 2-acetonaphthone of the formula ##STR5## wherein R 1 is H, halo or (C 1 -C 12 )alkoxy, acyloxy, carboxy, carbalkoxy, acyl, alkyl or thioalkyl, said process comprising heating at a temperature within the range of 150° C. to 800° C. and a pressure within the range of about 0.1 mmHg to 3 atm a compound selected from the group consisting of a ketal of the formula ##STR6## wherein R 1 is described above, and each R 2 is (C 1 -C 12 )alkyl or the two R 2 taken together are (C 2 -C 12 )alkylene, or an enol ether of the formula ##STR7## wherein R 1 is as defined above and R 2 is (C 1 -C 12 )alkyl or C 2 -C 12 acyl at a temperature effective to cyclize the compound and obtain said 2-acetonaphthones.

Claim 3

The process of claim 1, wherein the heating is conducted in the vapor phase.

Claim 4

The process of claim 1, wherein the temperature is about 350° to 600° C., and the pressure is about 0.1 mmHg to atmospheric pressure.

Claim 5

The process of claim 1, wherein the heating is conducted in the presence of a solvent at a temperature of about 175° to 300° C.

Claim 6

The process of claim 4, wherein the solvent has a normal boiling point which is higher than the same as the reaction temperature.

Claim 7

The process of claim 4, wherein the solvent has a normal boiling point which is lower than the reaction temperature; and the reaction is conducted under a pressure higher than about atmospheric pressure.

Claim 8

The process of claim 1, wherein the compounds heated is said ketal.

Claim 9

The process of claim 7, further comprising distilling the ketal prior to said heating step.

Claim 10

The process of claim 7, wherein the heating step is conducted by heating the ketal at a temperature of about 75° to 300° C. to obtain an enol ether of the benzalacetone; and then heating the enol ether at a temperature effective to cyclize said enol ether and obtain said 2-acetonaphthone.

Claim 11

The process of claim 9, wherein the heating of the enol ether is conducted in the vapor phase at a temperature of about 150° to 800° C.

Claim 12

The process of claim 10, wherein the temperature is about 350° to 600° C.

Claim 13

The process of claim 9, wherein the heating of the enol ether is conducted in an inert solvent at a temperature of about 175° to 300° C.

Claim 14

The process of claim 12, wherein the solvent has a normal boiling point which is higher than or the same as the reaction temperature.

Claim 15

The process of claim 12, wherein the solvent has a normal boiling point which is lower than about the reaction temperature; and the reaction is conducted under a pressure greater than about atmospheric pressure.

Claim 16

A process for preparing a 2-acetonaphthones of the formula ##STR8## wherein R 1 is H, halo or (C 1 -C 12 )alkoxy, acyloxy, carboxy, carbalkoxy, acyl, alkyl or thioalkyl, said process comprising reacting at a temperature in the range of -25° to 250° C. an acyl-substituted benzalacetone of the formula ##STR9## wherein R 1 is as defined above, with a ketalizing agent selected from the group consisting of alkyl glycols and di-alkyl acetals, di-alkyl ketals, and tri-alkyl orthoesters; said benzalacetone and said ketalizing agent being present in a proportion and under conditions effective to form a compound selected from the group consisting of a ketal of an acetyl-substituted benzalacetone of the formula ##STR10## wherein R 1 is as defined above, and R 2 is (C 1 -C 12 )alkyl or the two R 2 taken together are (C 1 -C 12 )alkylene, or an enol ether of an acetyl-substituted benzalacetone of the formula ##STR11## wherein R 1 is as defined above and R 2 is (C 1 -C 12 )alkyl or (C 2 -C 12 )acyl and heating said compound at a temperature effective to cyclize said compound and form said 2-acetonaphthone.

Claim 17

A process for preparing a 2-acetonaphthones of the formula ##STR8## wherein R 1 is H, halo or (C 1 -C 12 )alkoxy, acyloxy, carboxy, carbalkoxy, acyl, alkyl or thioalkyl, said process comprising reacting at a temperature in the range of -25° to 250° C. an acyl-substituted benzalacetone of the formula ##STR9## wherein R 1 is as defined above, with a ketalizing agent selected from the group consisting of alkyl glycols and di-alkyl acetals, di-alkyl ketals, and tri-alkyl orthoesters; said benzalacetone and said ketalizing agent being present in a proportion and under conditions effective to form a compound selected from the group consisting of a ketal of an acetyl-substituted benzalacetone of the formula ##STR10## wherein R 1 is as defined above, and R 2 is (C 1 -C 12 )alkyl or the two R 2 taken together are (C 1 -C 12 )alkylene, or an enol ether of an acetyl-substituted benzalacetone of the formula ##STR11## wherein R 1 is as defined above and R 2 is (C 1 -C 12 )alkyl or (C 2 -C 12 )acyl and heating said compound at a temperature effective to cyclize said compound and form said 2-acetonaphthone.

Claim 18

The process of claim 15, wherein the reaction of the benzalacetone with the ketalizing agent is conducted in the presence of an acid catalyst.

Claim 19

The process of claim 16, wherein the acid is an acidic resin.

Claim 20

A process for producing a 2-acetonaphthone of the formula ##STR12## wherein R 1 is H, halo or (C 1 -C 12 )alkoxy, acyloxy, carboxy, carbalkoxy, acyl, alkyl or thioalkyl, and R 1 is H, (C 1 -C 12 )alkyl, (C 6 -C 20 )aryl, (C 7 -C 21 )alkaryl or araalkyl, said process comprising reacting at a temperature within the range of 350° C. to 600° C. and a pressure within the range of about 0.1 mmHg to atmospheric pressure acetylacetone with a benzaldehyde substituted with H, halo or, (C 1 -C 12 )alkyl, carboxy, carbalkoxy, acyloxy, acyl, alkoxy or alkylthio; said diketone and said benzaldehyde being present in a proportion and under conditions effective to form an acyl-substituted benzalacetone of the formula ##STR13## wherein R 1 is as defined above; reacting said benzalacetone with a ketalizing agent selected from the group consisting of alkyl glycols and di-alkyl acetals, di-alkyl ketals, and tri-alkyl orthoesters; said benzalacetone and said ketalizing agent being present in a proportion and under conditions effective to form a compound selected from the group consisting of a ketal of said benzalacetone of the formula ##STR14## wherein R 1 is as defined above, and R 2 is (C 1 -C 12 )alkyl or the two R 2 taken together are (C 1 -C 12 )alkylene, or an enol ether of said benzalacetone of the formula ##STR15## wherein R 1 is as defined above and R 2 is (C 1 -C 12 )alkyl or (C 2 -C 12 )acyl, and heating said compound at a temperature effective to cyclize said compound and form said 2-acetonaphthone.

Claim 21

A process for producing a 2-acetonaphthone of the formula ##STR12## wherein R 1 is H, halo or (C 1 -C 12 )alkoxy, acyloxy, carboxy, carbalkoxy, acyl, alkyl or thioalkyl, and R 1 is H, (C 1 -C 12 )alkyl, (C 6 -C 20 )aryl, (C 7 -C 21 )alkaryl or araalkyl, said process comprising reacting at a temperature within the range of 350° C. to 600° C. and a pressure within the range of about 0.1 mmHg to atmospheric pressure acetylacetone with a benzaldehyde substituted with H, halo or, (C 1 -C 12 )alkyl, carboxy, carbalkoxy, acyloxy, acyl, alkoxy or alkylthio; said diketone and said benzaldehyde being present in a proportion and under conditions effective to form an acyl-substituted benzalacetone of the formula ##STR13## wherein R 1 is as defined above; reacting said benzalacetone with a ketalizing agent selected from the group consisting of alkyl glycols and di-alkyl acetals, di-alkyl ketals, and tri-alkyl orthoesters; said benzalacetone and said ketalizing agent being present in a proportion and under conditions effective to form a compound selected from the group consisting of a ketal of said benzalacetone of the formula ##STR14## wherein R 1 is as defined above, and R 2 is (C 1 -C 12 )alkyl or the two R 2 taken together are (C 1 -C 12 )alkylene, or an enol ether of said benzalacetone of the formula ##STR15## wherein R 1 is as defined above and R 2 is (C 1 -C 12 )alkyl or (C 2 -C 12 )acyl, and heating said compound at a temperature effective to cyclize said compound and form said 2-acetonaphthone.