反応 #2460310

ord-21a8a337476c4837b49a66abafd425a3

反応方程式

CCCCOC(=O)c1ccc(-c2ccc(C(F)(F)F)cc2)cc1
butyl 4′-(trifluoromethyl)biphenyl-4-carboxylate
CCCCOC(=O)c1cccc(I)c1
butyl 3-iodobenzoate
CCCCOC(=O)c1cccc(-c2ccc(C(F)(F)F)cc2)c1
butyl 4′-(trifluoromethyl)biphenyl-3-carboxylate
収率 40.0%

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他The product was purified by column chromatography
  2. 2
    workup.DISTILLATIONfollowed by vacuum distillation
  3. 3
    その他collecting fraction bp 127-131° C./0.12 mm
  4. 4
    その他obtained in 40% yield

実験手順

This compound was prepared by the procedure for butyl 4′-(trifluoromethyl)biphenyl-4-carboxylate (CS-16), except using butyl 3-iodobenzoate instead of butyl 4-iodobenzoate. The product was purified by column chromatography followed by vacuum distillation, collecting fraction bp 127-131° C./0.12 mm. The product was a colorless oil, and obtained in 40% yield. 1H NMR (CDCl3): δ 0.99 (t, 3H), 1.5 (m, 2H), 1.8 (m, 2H), 4.37 (t, 2H), 7.54 (d, 2H), 7.72 (s, 4H), 7.77 (d, 2H), 8.09 (d, 2H), 8.28 (s, 2H).

出典

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