2-Hydroxy-5-nitrobenzyl alcohol → (5-Nitro-2-propoxyphenyl)methanol
反応式
[N+:1]([C:4]1[CH:5]=[CH:6][C:7]([O:12][CH2:13][CH2:14][CH3:15])=[C:8]([CH:11]=1)[CH:9]=[O:10])([O-:3])=[O:2].OCC1C=C([N+]([O-])=O)C=CC=1O>>[N+:1]([C:4]1[CH:5]=[CH:6][C:7]([O:12][CH2:13][CH2:14][CH3:15])=[C:8]([CH:11]=1)[CH2:9][OH:10])([O-:3])=[O:2]参加物
3
実験手順
This compound was prepared by reduction of 5-nitro-2-propyloxybenzaldehyde using a method similar to that described for preparing 2-hydroxymethyl-4-nitrophenol in 93% yield: MP (No Sample left for MP); 1H NMR (400 MHz, DMSO-d6) 8.22 (d, 1H, J=2.6 Hz), 8.13 (dd, 1H, J=2.9 and 9.2 Hz), 7.14 (d, 1H, J=9.2 Hz), 5.41 (t, 1H, J=5.5 Hz), 4.52 (d, 2H, J=5.8 Hz), 4.08 (t, 2H, J=6.2), 1.75 (m, 2H), 0.98 (t, 3H, J=7.6 Hz).
後処理
- waitMP (No Sample left for MP)
出典と根拠
- ORDレコード
- ord-a669a824ca8941f2a137221769d55ed0
- 出典データセット
- uspto-grants-2010_08
- 特許番号
- US07772216B2
反応ノート
読み込み中…