反应 #1005994

ord-101e256fa83c4725a1835d9fd76c8208

反应方程式

Nc1ccc(C(F)(F)F)cc1
4-aminobenzotrifluoride
COC(=O)c1cccc(Br)c1
methyl 3-bromobenzoate
COC(=O)c1cccc(Nc2ccc(C(F)(F)F)cc2)c1
3-[N-(4-Trifluoromethylphenyl)amino]benzoic acid methyl ester

反应条件

详细条件
See reaction.notes.procedure_details.

实验过程

Reaction of methyl 3-bromobenzoate with 4-aminobenzotrifluoride according to general procedure A provided methyl ester of Compound 7 as a white solid (86% yield). 1H NMR (CDCl3, 500 MHz): δ=7.82 (s, 1H), 7.71 (d, J=7.6 Hz, 1H), 7.50 (d, J=8.4 Hz, 2H), 7.40 (t, J=7.8 Hz, 1H), 7.33 (m, 1H), 7.08 (d, J=8.5 Hz, 2H), 6.11 (bs, 1H), 3.93 (s, 3H). 13C NMR (CDCl3, 125 MHz): δ=167.0, 146.3, 141.9, 131.8, 129.8, 127.0, 123.9, 120.5, 116.1, 52.5.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US09271961B2uspto-grants-2016_03