反応 #11172

ord-a45e48d54ee2440894b7512541d2c34c

反応方程式

Cc1ccccc1C#N
o-tolunitrile
CC(C)(C#N)N=NC(C)(C)C#N.O=C1CCC(=O)N1Br
NBS AIBN
[Br-]
bromide
c1ccc(P(c2ccccc2)c2ccccc2)cc1
triphenylphosphine
N#Cc1ccccc1C[P+](c1ccccc1)(c1ccccc1)c1ccccc1.[Br-]
phosphonium
収率 70.0%
N#Cc1ccccc1C[P+](c1ccccc1)(c1ccccc1)c1ccccc1.[Br-]
(2-Cyanobenzyl)(triphenyl)phosphonium bromide
収率 70.0%

反応条件

詳細条件
See reaction.notes.procedure_details.

実験手順

Bromination of o-tolunitrile with NBS/AIBN, followed by reaction of the crude bromide with triphenylphosphine (1.2 equiv.), using the procedure described in example 102, except that the reaction time for the bromination was 2 h, gave the phosphonium salt (547) (70%) as a light brown powder, mp (CH2Cl2/benzene) 237–241° C. 1H NMR (CDCl3) δ 7.90 (dd, J=7.8, 2.3 Hz, 1H), 7.85–7.63 (m, 15H), 7.52 (br t, J=7.7 Hz, 1H), 7.44 (br d, J=7.5 Hz, 1H), 7.38 (tdd, J=7.6, 2.1, 1.0 Hz, 1H), 5.86 (d, J=14.7 Hz, 2H). Found: C, 67.88; H, 4.42; N, 3.09. C26H21BrNP requires C, 68.13; H, 4.62; N, 3.06.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US07094798B1uspto-grants-2006_08