تفاعل #3027

ord-9d4147d3edea46ffb150787b3152cac8

معادلة التفاعل

Cc1ccc(Cl)cc1C
4-chloro-o-xylene
O=C(c1ccc2c(c1)C(=O)OC2=O)c1ccc2c(c1)C(=O)OC2=O
3,3',4,4'-benzophenonetetracarboxylic dianhydride
O=C(Cl)C(=O)Cl
oxalyl chloride
Cc1cc(Cl)c(C(=O)c2cc(C)c(C)cc2Cl)cc1C
2,2'dichloro-4,4',5,5',-tetramehtylbenzophenone

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىare readily available from commercial sources or synthesis

الإجراء التجريبي

Specific benzophenonetetracarboxylic dianhydrides preferred in this invention are readily available from commercial sources or synthesis. For instance, 3,3',4,4'-benzophenonetetracarboxylic dianhydride (D1) is available from Aldrich Chemical Co., Inc. (1001 W. St. Paul Ave., Milwaukee, Wis. 53233). 2,2'-Dichloro-4,4',5,5'-benzophenone tetracarboxylic dianhydride (D2) is available from 4-chloro-o-xylene by Friedel-Crafts acylation with oxalyl chloride to give 2,2'dichloro-4,4',5,5',-tetramehtylbenzophenone, followed by oxidation with nitric acid and dehydration of the resulting tetracarboxylic acid as described by Falcigno, et al., J. Poly. Sci. 1992, 30, 1433.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05731405uspto-grants-1998_03