تفاعل #886

ord-a9328cbc649c44739edcb5b4674d8842

معادلة التفاعل

C=C
ethylene
Brc1ccccc1
bromobenzene
O=C(Cl)/C=C/C(=O)Cl
fumaryl chloride
Brc1ccc(-c2ccc(-c3ccc(Br)cc3)o2)cc1
2,5-Bis(p-bromophenyl) furan

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةthe mixture was heated to reflux
  2. 2
    درجة الحرارةrefluxing
  3. 3
    ترشيحfiltered
  4. 4
    أخرىRecrystallization from acetic acid
  5. 5
    أخرىgave 5.6 g (75%), mp 198°-199° C. (lit. (R. E. Lutz and W. M. Eisner, J. Am. Chem. Soc. 56, 2698 (1934)) mp 200°-201° C.)

الإجراء التجريبي

A literature procedure as known in the art for preparation of trans-di-p-bromobenzoylethylene from bromobenzene and fumaryl chloride was employed. J. B. Conant and R. E. Lutz, J. Am. Chem. Soc. 47, 881 (1925). The ethylene compound was reduced with Zn-HOAc to prepare 1,4-di-p-bromophenyl-1,4-butanedione. E. Campaigne and W. O. Foye, J. Org. Chem. 17, 1405 (1952). The saturated 1,4-diketone (7.9 g, 0.02 mol) was suspended in 80 mL of AC2O and the mixture was heated to reflux. Concentrated H2SO4 (4-5 drops) was added and refluxing was continued for 5 min. The solution was poured into water-ice (1 L), stirred well, and filtered: crude yield 7 g (93%). Recrystallization from acetic acid gave 5.6 g (75%), mp 198°-199° C. (lit. (R. E. Lutz and W. M. Eisner, J. Am. Chem. Soc. 56, 2698 (1934)) mp 200°-201° C.).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05723288uspto-grants-1998_03