反应 #2460308

ord-05aa77f53f204125947efc3a9d2b19d2

反应方程式

CCCCOC(=O)c1ccc(-c2ccc(C(=O)OCCCC)cc2-c2ccccc2)cc1
dibutyl 4,4′-terphenyl dicarboxylate
CCCCOC(=O)c1cccc(I)c1
butyl 3-iodobenzoate
CCCCOC(=O)c1cccc(-c2cccc(C(=O)OCCCC)c2-c2ccccc2)c1
dibutyl 3,3′-terphenyl dicarboxylate

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    workup.DISTILLATIONpurified by vacuum distillation
  2. 2
    其他collecting the fraction bp 104-108° C./0.2 mm
  3. 3
    其他A colorless oil was obtained

实验过程

This compound was prepared by the procedure for dibutyl 4,4′-terphenyl dicarboxylate (CS-13). The intermediate, butyl 3-iodobenzoate, was prepared and purified by vacuum distillation, collecting the fraction bp 104-108° C./0.2 mm. A colorless oil was obtained, mass: 26.17 g (85% of theory). 1H NMR (CDCl3): δ 0.98 (t, 3H), 1.5 (m, 2H), 1.8 (m, 2H), 4.32 (q, 2H), 7.18 (t, 1H), 7.88 (d, 1H), 8.00 (d, 1H), 8.36 (s, 1H).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07459263B2uspto-grants-2008_12