反応式
[C:1]1([CH:7]([C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][C:11]=2C)[CH2:8][NH2:9])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[Br:17]C1C=CC=CC=1C(C1C=CC=CC=1)=O>>[Br:17][C:11]1[CH:12]=[CH:13][CH:14]=[CH:15][C:10]=1[CH:7]([C:1]1[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1)[CH2:8][NH2:9]参加物
3
実験手順
The title material was prepared as described for the synthesis of 2-phenyl-2-o-tolylethanamine (Example FF) in using (2-bromophenyl)(phenyl)methanone. 1H NMR (400 MHz, DMSO-d6) δ ppm: 3.15 (2H, dd, J=7.45, 2.65 Hz) 4.36 1H, (t, J=7.45 Hz) 7.12-7.20 (2H, m) 7.22-7.29 (5H, m) 7.38 (1H, td, J=7.52, 1.14 Hz) 7.48 (1H, dd, J=7.71, 1.64 Hz) 7.58 (1H, dd, J=7.83, 1.26 Hz).
出典と根拠
- ORDレコード
- ord-51d866667bc6420e923561b7095dffbf
- 出典データセット
- uspto-grants-2012_04
- 特許番号
- US08148400B2
関連ノート
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