Monomer for a hardmask composition, hardmask composition comprising the monomer, and method for forming a pattern using the hardmask composition
a technology of composition and monomer, which is applied in the direction of photomechanical instruments, originals for photomechanical treatment, photomechanical apparatus, etc., can solve the problem of difficult to provide a fine pattern with an excellent profile, and achieve the effect of ensuring dissolubility
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synthesis example 1
First Step: Friedel-Craft Acylation Reaction
[0075]50.0 g (0.166 mol) of coronene, 28.4 g (0.1666 mol) of 4-methoxybenzoylchloride, and 235 g of 1,2-dichloroethane were put in a flask, preparing a solution. Then, 22.2 g (0.166 mol) of aluminum chloride was slowly added to the solution at room temperature. The mixture was heated up to 60° C. and then, agitated for 8 hours. When the reaction was complete, methanol was added to the agitated solution. Then, a precipitate produced therein was filtrated, obtaining 4-methoxybenzoyl coronene.
Second Step: Demethylation
[0076]50.0 g (0.115 mol) of the 4-methoxybenzoyl coronene obtained in the first step, 58.2 g (0.288 mol) of 1-dodecanethiol, 19.4 g (0.345 mol) of potassium hydroxide, and 191 g of N,N-dimethylformamide was put in a flask, and the mixture was agitated for 120° C. for 8 hours. The agitated mixture was cooled down, neutralized with a 10% hydrogen chloride solution into about pH 7, and extracted with ethyl acetate, obtaining 4-hydr...
synthesis example 2
First Step: Friedel-Craft Acylation Reaction
[0078]50.0 g (0.166 mol) of coronene, 56.8 g (0.333 mol) of 4-methoxybenzoylchloride, and 353 g of 1,2-dichloroethane were put in a flask, preparing a solution. Then, 44.4 g (0.333 mol) of aluminum chloride was slowly added to the solution at room temperature, and the mixture was heated up to 60° C. and agitated for 8 hours. When the reaction was complete, methanol was added to the solution. Then, a precipitate produced therein was filtrated, obtaining double substituted 4-methoxybenzoyl coronene.
Second Step: Demethylation
[0079]50.0 g (0.880 mol) of the double substituted 4-methoxybenzoyl coronene obtained in the first step, 89.0 g (0.440 mol) of 1-dodecanethiol, 29.6 g (0.528 mol) of potassium hydroxide, and 253 g of N,N-dimethylformamide were put in a flask. The mixture was agitated at 120° C. for 8 hours. Then, the agitated mixture was cooled down, neutralized with a 10% hydrogen chloride solution into about pH 7, and extracted with eth...
synthesis example 3
First Step: Friedel-Craft Acylation Reaction
[0081]50.0 g (0.166 mol) of coronene, 85.2 g (0.499 mol) of 4-methoxybenzoylchloride, and 471 g of 1,2-dichloroethane were put in a flask, preparing a solution. Then, 66.6 g (0.499 mol) of aluminum chloride was slowly added to the solution at room temperature. The mixture was heated up to 60° C. and agitated for 8 hours. When the reaction was complete, methanol was added to the solution. Then, a precipitate produced therein was filtrated triple substituted 4-methoxybenzoyl coronene.
Second Step: Demethylation
[0082]50.0 g (0.0712 mol) of the triple substituted 4-methoxybenzoyl coronene flask obtained in the first step, 108.0 g (0.534 mol) of 1-dodecanethiol, 35.9 g (0.640 mol) of potassium hydroxide, and 291 g of N,N-dimethylformamide were put in a flask. The mixture was agitated at 120° C. and agitated for 8 hours. Then, the agitated mixture was cooled down, neutralized with a 10% hydrogen chloride solution into about pH 7, and extracted wi...
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