反応式
[CH3:1][C:2]1[CH:10]=[C:9]([C:11]([OH:13])=[O:12])[CH:8]=[CH:7][C:3]=1[C:4]([OH:6])=O>CO>[O:6]=[C:4]1[C:3]2[CH:7]=[CH:8][C:9]([C:11]([OH:13])=[O:12])=[CH:10][C:2]=2[CH:1]=[CH:1][C:2]2[CH:10]=[CH:9][CH:8]=[CH:7][C:3]1=2参加物
実験手順
5-Oxo-5H-dibenzo[a,d]cycloheptene-2-carboxylic acid is prepared by esterifying 2-methylterephthalic acid with methanol, in the presence of acid catalyst, to afford the corresponding dimethyl ester which, in turn, is reacted with N-bromosuccinimide to afford 2-bromomethylterephthalic acid dimethyl ester. This diester is reacted with triphenylphosphine to afford 2,5-bis(carbomthoxy)benzyltriphenyl-phosphonium bromide which is treated with benzaldehyde and diazabicylononene, to afford, after alkaline hydroylsis, cis and trans stilbene 2,5-dicarboxylic acid. Hydrogenation of this latter compound with hydrogen over a 5% palladium on carbon catalyst affords 2-(2-phenethyl)terephthalic acid. Treatment with polyphosphoric acid yields 5-oxo-5H-dibenzo[a,d]-cycloheptane-2-carboxylic acid which can be recrystallized from aqueous dimethylformamide. 5-Oxo-5H-dibenzo[a,d]cycloheptene-2-carboxylic acid is prepared by successively treating 5-oxo-5H-dibenzo[a,d]cycloheptane-2-carboxylic acid with diazomethane, N-bromosuccinimide, and dimethylformamide/diazabicyclononene, followed by base hydrolysis and acidification.
出典と根拠
- ORDレコード
- ord-a61cc78cb56a4e74b6cfbf1f4627080d
- 出典データセット
- uspto-grants-1976_08
- 特許番号
- US03975540
関連ノート
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